Steroid sulphatase inhibitors

ABSTRACT

A method of inhibiting steroid sulphatase activity in a subject in need of same is described. 
     The method comprises administering to said subject a steroid sulphatase inhibiting amount of a ring system compound; which ring system compound comprises a ring to which is attached a sulphamate group of the formula 
                 
 
wherein each of R 1  and R 2  is independently selected from H, alkyl, alkenyl, cycloalkyl and aryl, or together represent allylene optionally containing one or more hetero atoms or groups in the alkylene chain; and wherein said compound is an inhibitor of an enzyme having steroid sulphatase activity (E.C.3.1.6.2); and if the sulphamate group of said compound is replaced with a sulphate group to form a sulphate compound and incubated with a steroid sulphatase enzyme (E.C.3.1.6.2) at a pH 7.4 and 37° C. it would provide a K m  value of less than 50 μM.

RELATED APPLICATIONS

This application is a division of prior application Ser. No. 09/579,163,filed May 25, 2000 which is a divisional of U.S. Ser. No. 09/238,345, filed Jan. 27, 1999, now U.S. Pat. No. 6,187,766; U.S. application Ser. No. 09/238,345 was a division of U.S. application Ser. No. 09/111,927, filed Jul. 8, 1998, incorporated herein by reference and now U.S. Pat. No. 6,011,024, which in turn was a continuation-in-part of U.S. application Ser. No. 08/458,352, filed Jun. 2, 1995, now U.S. Pat. No. 5,830,886, which was a division of U.S. application Ser. No. 08/196,192, filed (§102(e) date of) Dec. 27, 1994, now U.S. Pat. No. 5,616,574. U.S. application Ser. No. 08/196,192 was the U.S. National Phase of PCT/GB92/01587, filed Aug. 28, 1992 and designating the U.S., and incorporated herein by reference. U.S. application Ser. No. 08/196,192 has a §371 date of Dec. 27, 1994 and a §102(e) date of Dec. 27, 1994. PCT/GB92/01587 was published as WO93/05064, has a publication date of Mar. 18, 1993, and claims priority from United Kingdom patent application No. 9118478, filed Aug. 29, 1991. U.S. Ser. No. 09/111,927 was also a continuation-in-part of PCT patent application number PCT/GB97/00600, filed Mar. 4, 1997, designating the U.S., and claiming priority from United Kingdom patent applications 9604709.7 and 9605725.2, filed Mar. 5 and 19, 1996, respectively. PCT/GB97/00600 was published as WO 97/32872 on Sep. 12, 1997. U.S. Ser. No. 09/111,927 was also a continuation-in-part of PCT patent application number PCT/GB97/00444, filed Feb. 17, 1997, designating the U.S., and claiming priority from United Kingdom patent application 9603325.3, filed Feb. 16, 1996. PCT/GB97/00444 was published as WO 97/30041 on Aug. 21, 1997. U.S. Ser. No. 09/111,927 was also a continuation-in-part of PCT patent application number PCT/GB97/03352, filed Dec. 4, 1997, designating the U.S., and claiming priority from United Kingdom patent application 9625334.9, filed Dec. 5, 1996. PCT/GB97/03352 was published as WO 98/24802 on Jun. 11, 1998. Each of PCT/GB97/00600 (WO 97/32872), PCT/GB97/00444 (WO 97/30041), and PCT/GB97/03352 (WO 98/24802) is hereby incorporated herein by reference.

FIELD OF INVENTION

This invention relates to novel compounds for use as steroid sulphatase inhibitors, and pharmaceutical compositions containing them.

BACKGROUND AND PRIOR ART

Steroid precursors, or pro-hormones, having a sulphate group in the 3-position of the steroid nucleus, referred to hereinafter simply as steroid sulphates, are known to play an important part as intermediates in steroid metabolism in the human body. Oestrone sulphate and dehydroepiandrosterone (DHA) sulphate, for example, are known to play an important role as intermediates in the production, in the body, of oestrogens such as oestrone and oestradiol. Oestrone sulphate, in particular, is known, for example, to represent one of the major circulating oestrogen precursors particularly in post-menopausal women and oestrone sulphatase activity in breast tumours is 100-1000 fold greater than that of other enzymes involved, in oestrogen formation (James et al., Steroids, 50, 269-279 (1987)).

Not only that, but oestrogens such as oestrone and oestradiol, particularly the over-production thereof, are strongly implicated in malignant conditions, such as breast cancer, see Breast Cancer, Treatment and Prognosis: Ed. R. A. Stoll, pp. 156-172, Blackwell Scientific Publications (1986), and the control of oestrogen production is the specific target of many anti-cancer therapies, both chemotherapy and surgical, e.g. oöphorectomy and adrenalectomy. So far as endocrine therapy is concerned, efforts have so far tended to concentrate on aromatase inhibitors, i.e. compounds which inhibit aromatase activity, which activity is involved, as the accompanying oestrogen metabolic flow diagram (FIG. 1) shows, in the conversion of androgens such as androstenedione and testosterone to oestrone and oestradiol respectively.

In recently published International Application WO91/13083 a proposal has been made to target a different point in the oestrogen metabolic pathway, or rather two different points, that is to say the conversion of DHA sulphate and oestrone sulphate to DHA and oestrone, respectively, by steroid sulphatase activity, and using 3-monoalkylthiophosphonate steroid esters as a steroid sulphatase inhibitor, more especially oestrone-3-monomethylthiophosphonate.

OBJECTS OF THE INVENTION

A first object of the present invention is to provide new compounds capable of inhibiting steroid sulphatase activity in vitro and in vivo.

A second object of the present invention is to provide new compounds having improved activity as steroid sulphatase inhibitors both in vitro and in vivo.

A third object of the invention is to provide pharmaceutical compositions effective in the treatment of oestrogen dependent tumours.

A fourth object of the invention is to provide pharmaceutical compositions effective in the treatment of breast cancer.

A fifth object of the invention is to provide a method for the treatment of oestrogen dependent tumours in mammals, especially humans.

A sixth object of the invention is to provide a method for the treatment of breast cancer in mammals and especially in women.

SUMMARY OF INVENTION

The invention is based on the discovery of novel compounds having steroid sulphatase inhibitory activity, in some cases, with extremely high activity levels.

In one aspect, the present invention provides a method of inhibiting steroid sulphatase activity in a subject in need of same.

In another aspect, the present invention provides compounds and compositions useful in that method of inhibiting steroid sulphatase activity.

The method of the present invention comprises administering to said subject a steroid sulphatase inhibiting amount of a ring system compound; which ring system compound comprises a ring to which is attached a sulphamate group of the formula

wherein each of R₁ and R₂ is independently selected from H, alkyl, alkenyl, cycloalkyl and aryl, or together represent alkylene optionally containing one or more hetero atoms or groups in the alkylene chain; and wherein said compound is an inhibitor of an enzyme having steroid sulphatase activity (E.C.3.1.6.2); and if the sulphamate group of said compound is replaced with a sulphate group to form a sulphate compound and incubated with a steroid sulphatase enzyme (E.C.3.1.6.2) at a pH 7.4 and 37° C. it would provide a K_(m) value of less than 50 μM.

The compounds that are useful in the method of the present invention are sulphamic acid ester ring system compounds, the sulphate of which is a substrate for enzymes having steroid sulphatase (EC 3.1.6.2) activity, the N-alkyl and N-aryl derivatives of those sulphamic acid esters, and their pharmaceutically acceptable salts.

In one aspect of the present invention, compounds for use in the method of the present invention are the sulphamic acid esters of polycyclic alcohols, being polycyclic alcohols the sulphate of which is a substrate for enzymes having steroid sulphatase (EC 3.1.6.2) activity, the N-alkyl and N-aryl derivatives of those sulphamic acid esters, and their pharmaceutically acceptable salts.

For one aspect of the present invention, broadly speaking, the novel compounds of this invention are compounds of the Formula (I)

where:

-   -   R₁ and R₂ are each independently selected from H, alkyl,         cycloalkyl, alkenyl and aryl, or together represent alkylene         optionally containing one or more hetero atoms or groups in the         allylene chain; and     -   the group —O-Polycycle represents the residue of a polycyclic         alcohol, the sulphate of which is a substrate for enzymes having         steroid sulphatase activity (EC 3.1.6.2).

As used herein the reference to polycyclic alcohols, the sulphate of which is a substrate for enzymes having steroid sulphatase activity refers to polycyclic alcohols, the sulphate of which, viz: the derivatives of the Formula:

when incubated with steroid sulphatase EC 3.1.6.2 at pH 7.4 and 37° C. provides a K_(m) value of less than 50 μmoles.

BRIEF DESCRIPTION OF DRAWINGS

The activity of the present compounds as steroid sulphatase inhibitors is illustrated in the accompanying drawings, in which:

FIG. 1 is a schematic chart showing the metabolic pathways, enzymes and steroid intermediates associated with the production of oestradiol in vivo.

FIG. 2 is a histogram showing the dose-dependent inhibitory effect of oestrone-3-sulphamate on steroid sulphatase activity in human MCF-7 cells in vitro.

FIG. 3 is a histogram showing the dose-dependent inhibitory effect of oestrone-3-N,N-dimethylsulphamate on steroid sulphatase activity in human MCF-7 cells in vitro.

FIG. 4 is a graph comparing the log dose-response curves for oestrone-3-sulphamate and oestrone-3-N,N-dimethylsulphamate on steroid sulphatase activity in human MCF-7 cells in vitro.

FIG. 5 is a graph showing the dose-dependent inhibitory effect of oestrone-3-sulphamate, together with its IC₅₀ value (concentration required to produce 50% inhibition), on steroid sulphatase activity in human placental microsomes in vitro.

FIG. 6 shows the structures of oestrone (1), oestrone sulphate (2), oestrone-3-sulphamate (otherwise known as “EMATE”) (3) and steroid sulphamates (4-5) (See Example 13 and WO 97/30041).

FIG. 7 shows the structures of 7-hydroxycoumarin (11), 7-(sulphoxy)-4-methylcoumarin (12) and coumarin sulphamates (13-16) (See Example 13 and WO 97/30041).

FIG. 8 shows the sulphation of 7-hydroxy-4-methylcoumarin; pyridine/SO3-pyridine complex, NaOH in MeOH (Route a) (See Example 13 and WO 97/30041).

FIG. 9 shows the sulphamoylation of 7-hydroxy4-methylcoumarin; NaH/DMF, H2NSO2Cl in toluene (Route b) (See Example 13 and WO 97/30041).

FIG. 10 shows the dose-dependent inhibition of oestrone sulphatase in intact MCF-7 breast cancer cells by coumarin-7-O-sulphamate (13), 4-methylcoumarin-7-O-sulphamate (14), 3,4,8-trimethyl-coumarin-7-O-sulphamate (15) and 4-(trifluoromethyl)coumarin-7-O-sulphamate (16) (See Example 13 and WO 97/30041).

FIG. 11 shows the time-dependent and the concentration-dependent inactivation of oestrone sulphatase by 4-methyl-coumarin-7-O-sulphamate (14) (See Example 13 and WO 97/30041).

FIG. 12 is a graph (% inhibition vs. coumate) (See Example 13 and WO 97/30041).

FIGS. 13 and 14 present Formulae (A) to (H) with Formulae (A), (B) and (C) presented in FIG. 13 and Formulae (D), (E), (F), (G) and () presented in FIG. 14 (See Example 13. Preferably, in Formula (A), R₁-R₆ are independently selected from H, halo, hydroxy, sulphamate, alkyl and substituted variants or salts thereof; but wherein at least one of R₁-R₆ is a sulphamate group; and wherein X is any one of O, S, NH, a substituted N, CH₂, or a substituted C. Preferably X is O. Preferably, if the sulphamate group of the compound were to be replaced with a sulphate group to form a sulphate compound then that sulphate compound would be hydrolysable by an enzyme having steroid sulphatase (E.C. 3.1.6.2) activity. In a highly preferred embodiment, the compound is not hydrolysable by an enzyme having steroid sulphatase (E.C. 3.1.6.2) activity. In Formula (B) R₁-R₆ are independently selected from H, halo, hydroxy, sulphamate, alkyl and substituted variants or salts thereof; but wherein at least one of R1-R6 is a sulphamate group. The alkyl group(s) in Formula (A) or Formula (B) can be any suitable linear or branched alkyl group which may be saturated or unsaturated and/or substituted or non-substituted. The alkyl group may even be a cyclic alkyl group. For example, at least two of R₁-R₆ are linked to form a further cyclic component. Preferably R₁-R₅ are independently selected from H, alkyl and haloalkyl; preferably wherein R₁-R₅ are independently selected from H, C₁₋₆alkyl and C₁₋₆haloalkyl. Preferably R₁-R₅ are independently selected from H, C₁₋₃ alkyl and C1-3 haloalkyl. Preferably R₁-R₅ are independently selected from H, methyl and halomethyl. Preferably R₆ is OSO₂NH₂. In Formula (A) or Formula (B), two or more of R₁-R₆ may be linked together to form an additional cyclic structure. A typical example of such a compound has the general Formula (C), wherein any one of R₃-R₆ is a sulphamate group, and wherein n is an integer. Typically, R6 is a sulphamate group. A typical sulphamate group is —OS(O)(O)—NH₂. Preferably n is an integer of from 3 to 10, preferably from 3 to 7. Optionally, the group (CH₂)n of Formula (C) can be a substituted alkyl chain. Typical compounds falling within the general Formula (C) are shown in FIG. 14 as compound (D) (where n=3), compound (E) (where n=4), compound (F) (where n=5), compound (G) (where n=6), compound (H) (where n=7). For these compounds, R₆ is a sulphamate group of the formula —OS(O)(O)—NH₂ and each of R₃-R₅ is H. The term “sulphamate” includes an ester of sulphamic acid, or an ester of an N-substituted derivative of sulphamic acid, or a salt thereof. Thus, the term includes functional groups of the formula: —O—S(O)(O)—N(R₇)(R₈) where R₇ and R₈ are independently selected from H, halo, linear or branched alkyl which may be saturated or unsaturated and/or substituted or non-substituted, aryl, or any other suitable group. Preferably, at least one or R₇ and R₈ is H. In a preferred embodiment, each of R₇ and R₈ is H. See also WO 97/30041).

FIG. 15 shows a schematic diagram of some enzymes involved in the in situ synthesis of oestrone from oestrone sulfate, oestradiol and androstenedione (See Example 14 and WO 97/32872; see also FIG. 1. FIG. 15 shows the origin of oestrogenic steroids in postmenopausal women; “ER” denotes Oestrogen Receptor; “DHA/-S” denotes Dehydroepiandrosterone/-Sulfate; “DHA-STS” denotes DHA-sulphatase; “Adiol-STS” denotes Adiol Sulphatase; and “17B-HSD” denotes Oestradiol 17B-hydroxysteroid dehydrogenases).

FIGS. 16 a, 16 b, 16 c, and FIGS. 17 to 23 depict chemical formulae (See Example 14 and WO 97/32872. In a preferred embodiment, the compounds comprise a first ring structure and a sulphamoyl group, which first ring structure may be substituted and/or unsaturated. The first ring structure is preferably a phenolic ring structure, which may be substituted. The compounds may further comprise a second ring structure, which may be substituted and/or unsaturated. The compounds may preferably be a sulphamate of a flavone, an isoflavone or a flavanone, or a sulphamate of a benzoflavone, e.g., FIG. 23 wherein R is H or OH; and, the invention also encompasses substituted variants of the sulphamate of the benzoflavone of FIG. 23. With regard to FIGS. 16 a, 16 b, 16 c and 17 to 22, it is generally preferred that in formula I, A represents the first ring structure, B represents the third ring structure, D represents the second ring structure, C is an optional double bond, E is a link joining the second ring structure to the third ring structure, X represents a suitable first group, and Y represents a suitable second group, wherein any one of ring structures A, B, and D is a phenolic ring, and any one of ring structures A, B and D has bound thereto a sulphamate group. Each of the ring structures can independently comprise from 3 to 20 atoms in the ring, preferably 4 to 8 atoms in the ring; and, preferably ring A and ring D comprise 6 atoms in the ring. A further cyclic group may be linked to ring A or D. This cyclic group may be linked to two spaced-apart atoms in ring A or ring D, such as the structure shown in FIG. 23. Preferably the first ring structure and the second ring structure are substituted. Preferably any one of ring structures A and D has bound thereto a sulphamate group. Preferably, each of the first ring and the second ring is a homogeneous ring structure, i.e., the ring is made up of the same atoms. Preferably, each of the first ring and the second ring comprises only carbon atoms in the ring. Preferably X is C═O. Preferably the compound has the general formula II wherein F represents a phenolic ring structure (the first ring structure), J represents the third ring structure, I represents a phenolic ring structure (the second ring structure), G is an optional double bond, H is a link joining the second ring structure to the third ring structure, and Y represents a suitable second group, and any one of ring structures F, J and I has bound thereto a sulphamate group. Preferably the third ring structure is a heterogeneous ring structure, i.e., different atoms are in the ring. Preferably, Y is O. Preferably, any one of the ring structures F and I has bound thereto a sulphamate group. Preferably link E or link H is a bond. Preferably, the compound is a sulphamate of any one of a flavone, an isoflavone or a flavanone. Preferably, the compound is a compound of formula IV, V or VI, wherein R₁-R₁₂ are independently selected from H, OH, a halogen, an amine, an amide, a sulphonamine, a sulphonamide, any other sulphur containing group, a saturated or unsaturated C₁₋₁₀ alkyl, an aryl group, a saturated or unsaturated C₁₋₁₀ ether, a saturated or unsaturated C₁₋₁₀ ester, a phosphorus containing group, and wherein at least one of R₁-R₁₂ is a sulphamate group. Preferably the sulphamate group has the general formula OSO₂NR₁₃R₁₄ wherein R₁₃ and R₁₄ are independently selected from H, OH, a halogen, a saturated or unsaturated C₁₋₁₀ alkyl, an aryl group, a saturated or unsaturated C₁₋₁₀ ether, a saturated or unsaturated C₁₋₁₀ ester, and, each of R₁₃ and R₁₄ may be other suitable groups. Preferably the compound is a compound of formula IV, V or VI, wherein R₁-R₁₂ are independently selected from H, OH, OSO₂NR₁₃R₁₄, O—CH₃; wherein at least one of R₁-R₁₂ is OSO₂NR₁₃R₁₄ and R₁₃ and R₁₄ are as defined above. Preferably, at least one of R₁₃ and R₁₄ is H; and preferably each is H. Preferably, the compound is a sulphamate of any one of the flavone of formula VII, the isoflavone of formula VIII, or the flavanone of formula IX Preferably the compound is a sulphamate of any of formulae VII, VIII or IX. Preferably the compound is a sulphamate of a flavone, isoflavone or flavanone wherein the suphamoyl group is on the C4′ atom of the flavone, isoflavone or flavanone. The C4′ position is shown in formula III. Preferably, the compound is a flavonoid or flavanoid sulphamate. Preferably, if the sulphamate group of the compound were to be replaced with a sulphate group so as to form a sulphate compound then that sulphate compound would be hydrolysable by an enzyme having steroid sulphatase (E.C. 3.1.6.2) activity. The compound may have one or more sulphamate groups. For example, the compound may be mono-sulphamate or a bis-sulphamate. For instance, in FIGS. 20-22, R₃ and R₄ may be each a sulphamate).

FIG. 24 presents a bar graph of inhibition of oestrone sulphatase (See Example 14 and WO 97/32872).

FIGS. 25 to 34 show compounds of the Formulae I to X, respectively (See Example 15 and WO 98/24802. With reference to FIGS. 25 to 34: In Formula I; A is a first group; B is an aryl ring structure having at least 4 carbon atoms in the ring and wherein the ring B is substituted in at least the 2 position and/or the 4 position with an atom or group other than H; X is a sulphamate group; wherein group A and ring B together are capable of mimicking the A and B rings of oestrone; and wherein group A is attached to at least one carbon atom in ring B. The term “mimic” as used herein means having a similar or different structure but having a similar functional effect In other words, group A and ring B together of the compounds of the present invention are bio-isosteres of the A and B rings of oestrone. Preferably, the sulphamate group is at position 3 of the ring B. Preferably, the ring B has six carbon atoms in the ring. Preferably, the compound has the Formula II; wherein X is the sulphamate group; A is the first group; R₁ and/or R₂ is a substituent other than H; wherein R₁ and R₂ may be the same or different but not both being H; and wherein optionally group A is attached to at least one other carbon atom in ring B. Preferably, group A is additionally attached to the carbon atom at position 1 of the ring B. Preferably, group A and ring B are a steroid ring structure or a substituted derivative thereof. Preferably, the compound has the Formula IV; wherein X is the sulphamate group; R₁ and/or R₂ is a substituent other than H; wherein R₁ and R₂ may be the same or different but not both being H; and wherein Y is a suitable linking group. Suitable linking groups for Y include groups made up of at least any one or more of C, O, N, and S. The linking groups can also comprise H. The linking group may also increase the size of the ring (i.e. the D ring). Preferably, however, the D ring comprising Y is a five-membered ring. Preferably, Y is —CH₂— or —C(O)—. Preferably, Y is —C(O)—. Preferably, the compound has the Formula V; wherein X is the sulphamate group; R₁ and/or R₂ is a substituent other than H; and wherein R₁ and R₂ may be the same or different but not both being H. The term “sulphamate” as used herein includes an ester of sulphamic acid, or an ester of an N-substituted derivative of sulphamic acid, or a salt thereof. Preferably, the sulphamate group has the Formula III. In Formula III, each of R₃ and R₄ is independently selected from H or a hydrocarbyl group. The term “hydrocarbyl group” as used herein means a group comprising at least C and H and may optionally comprise one or more other suitable substituents. Examples of such substituents may include halo-, alkoxy-, nitro-, an alkyl group, a cyclic group etc. In addition to the possibility of the substituents being a cyclic group, a combination of substituents may form a cyclic group. If the hydrocarbyl group comprises more than one C then those carbons need not necessarily be linked to each other. For example, at least two of the carbons may be linked via a suitable element or group. Thus, the hydrocarbyl group may contain hetero atoms. Suitable hetero atoms will be apparent to those skilled in the art and include, for instance, sulphur, nitrogen and oxygen. A non-limiting example of a hydrocarbyl group is an acyl group. In one preferred embodiment of the present invention, the hydrocarbyl group for the sulphamate group is a hydrocarbon group. Here the term “hydrocarbon” means any one of an alkyl group, an alkenyl group, an alkynyl group, which groups may be linear, branched or cyclic, or an aryl group. The term hydrocarbon also includes those groups but wherein they have been optionally substituted. If the hydrocarbon is a branched structure having substituent(s) thereon, then the substitution may be on either the hydrocarbon backbone or on the branch; alternatively the substitutions may be on the hydrocarbon backbone and on the branch. Preferably, R₃ and R₄ are independently selected from H or alkyl, cycloalkyl, alkenyl and aryl, or together represent alkylene, wherein the or each alkyl or cycloalkyl or alkenyl or optionally contain one or more hetero atoms or groups. When substituted, the N-substituted compounds of this invention may contain one or two N-alkyl, N-alkenyl, N-cycloalkyl or N-aryl substituents, preferably containing or each containing a maximum of 10 carbon atoms. When R₃ and/or R₄ is alkyl, the preferred values are those where R₃ and R₄ are each independently selected from lower alkyl groups containing from 1 to 5 carbon atoms, that is to say methyl, ethyl, propyl etc. Preferably R₃ and R₄ are both methyl. When R₃ and/or R₄ is aryl, typical values are phenyl and tolyl (—PhCH₃; o-, m- or p-). Where R₃ and R₄ represent cycloalkyl, typical values are cyclopropyl, cyclopentyl, cyclohexyl etc. When joined together R₃ and R₄ typically represent an alkylene group providing a chain of 4 to 6 carbon atoms, optionally interrupted by one or more hetero atoms or groups, e.g. —O— or —NH— to provide a 5-, 6- or 7-membered heterocycle, e.g. morpholino, pyrrolidino or piperidino. Within the values alkyl, cycloalkyl, alkenyl and aryl Applicants include substituted groups containing as substituents therein one or more groups which do not interfere with the sulphatase inhibitory activity of the compound in question. Exemplary non-interfering substituents include hydroxy, amino, halo, alkoxy, alkyl and aryl. In some preferred embodiments, at least one of R₃ and R₄ is H. In some further preferred embodiments, each of R₃ and R₄ is H. Preferably, each of R₁ and R₂ is independently selected from H, alkyl, cycloalkyl, alkenyl, aryl, substituted alkyl, substituted cycloalkyl, substituted alkenyl, substituted aryl, any other suitable hydrocarbyl group, a nitrogen containing group, a S containing group, a carboxy containing group. Likewise, here, the term “hydrocarbyl group” means a group comprising at least C and H and may optionally comprise one or more other suitable substituents. Examples of such substituents may include halo-, alkoxy-, nitro-, an alkyl group, a cyclic group etc. In addition to the possibility of the substituents being a cyclic group, a combination of substituents may form a cyclic group. If the hydrocarbyl group comprises more than one C then those carbons need not necessarily be linked to each other. For example, at least two of the carbons may be linked via a suitable element or group. Thus, the hydrocarbyl group may contain hetero atoms. Suitable hetero atoms will be apparent to those skilled in the art and include, for instance, sulphur, nitrogen and oxygen. A non-limiting example of a hydrocarbyl group is an acyl group. Preferably, each of R₁ and R₂ is independently selected from H, C₁₋₆ alkyl, C₁₋₆ cycloalkyl, C₁₋₆ alkenyl, substituted C₁₋₆ alkyl, substituted C₁₋₆ cycloalkyl, substituted C₁₋₆ alkenyl, substituted aryl, a nitrogen containing group, a S containing group, or a carboxy group having from 1-6 carbon atoms. Likewise, here within the values alkyl, cycloalkyl, alkenyl and aryl Applicants include substituted groups containing as substituents therein one or more groups which do not interfere with the sulphatase inhibitory activity of the compound in question. Exemplary non-interfering substituents include hydroxy, amino, halo, alkoxy, alkyl and aryl. Preferably, each of R₁ and R₂ is independently selected from H, C₁₋₆ alkyl, C₁₋₆ alkenyl, a nitrogen containing group, or a carboxy group having from 1-6 carbon atoms. Preferably, each of R₁ and R₂ is independently selected from H, C₁₋₆ alkyl, C₁₋₆ alkenyl, NO₂, or a carboxy group having from 1-6 carbon atoms. Preferably, each of R₁ and R₂ is independently selected from H, C₃ alkyl, C₃ alkenyl, NO₂, or H₃CHO. Preferably, the compound is any one of the Formulae V-IX. Preferably, for some applications, the compound is further characterised by the feature that if the sulphamate group were to be substituted by a sulphate group to form a sulphate derivative, then the sulphate derivative would be hydrolysable by an enzyme having steroid sulphatase (E.C. 3.1.6.2) activity—i.e. when incubated with steroid sulphatase EC 3.1.6.2 at pH 7.4 and 37 C. In one preferred embodiment, if the sulphamate group of the compound were to be replaced with a sulphate group to form a sulphate compound then that sulphate compound would be hydrolysable by an enzyme having steroid sulphatase (E.C. 3.1.6.2) activity and would yield a K_(m) value of less than 50 mmoles when incubated with steroid sulphatase EC 3.1.6.2 at pH 7.4 and 37 C. In another preferred embodiment, if the sulphamate group of the compound were to be replaced with a sulphate group to form a sulphate compound then that sulphate compound would be hydrolysable by an enzyme having steroid sulphatase (E.C. 3.1.6.2) activity and would yield a K_(m) value of less than 50 μmoles when incubated with steroid sulphatase EC 3.1.6.2 at pH 7.4 and 37 C. In a highly preferred embodiment, the compound of the present invention is not hydrolysable by an enzyme having steroid sulphatase (E.C. 3.1.6.2) activity. Preferably the group A and the ring B together—hereinafter referred to as “group A/ring B combination”—will contain, inclusive of all substituents, a maximum of about 50 carbon atoms, more usually no more than about 30 to 40 carbon atoms. A preferred group A/ring B combination has a steroidal ring structure, that is to say a cyclopentanophenanthrene skeleton. Preferably, the sulphamyl or substituted sulphamyl group is attached to that skeleton in the 3-position. Thus, according to a preferred embodiment, the group A/ring B combination is a substituted or unsubstituted, saturated or unsaturated steroid nucleus. A suitable steroid nucleus is a substituted (i.e. substituted in at least the 2 and/or 4 position and optionally elsewhere in the steroid nucleus) derivative of any one of: oestrone, 2-OH-oestrone, 2-methoxy-oestrone, 4-OH-oestrone, 6a-OH-oestrone, 7a-OH-oestrone, 16a-OH-oestrone, 16b-OH-oestrone, oestradiol, 2-OH-17b-oestradiol, 2-methoxy-17b-oestradiol, 4-OH-17b-oestradiol, 6a-OH-17b-oestradiol, 7a-OH-17b-oestradiol, 16a-OH-17a-oestradiol, 16b-OH-17a-oestradiol, 16b-OH-17b-oestradiol, 17a-oestradiol, 17b-oestradiol, 17a-ethinyl-17b-oestradiol, oestriol, 2-OH-oestriol, 2-methoxy-oestriol, 4-OH-oestriol, 6a-OH-oestriol, 7a-OH-oestriol, dehydroepiandrosterone, 6a-OH-dehydroepiandrosterone, 7a-OH-dehydroepiandrosterone, 16a-OH-dehydroepiandrosterone, 16b-OH-dehydroepiandrosterone. In general terms the group A/ring B combination may contain a variety of non-interfering substituents. In particular, the group A/ring B combination may contain one or more hydroxy, alkyl especially lower (C₁-C₆) alkyl, e.g. methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, n-pentyl and other pentyl isomers, and n-hexyl and other hexyl isomers, alkoxy especially lower (C₁-C₆) alkoxy, e.g. methoxy, ethoxy, propoxy etc., alkenyl, e.g. ethenyl, or halogen, e.g. fluoro substituents. The group A/ring B combination may even be a non-steroidal ring system. A suitable non-steroidal ring system is a substituted (i.e. substituted in at least the 2 and/or 4 position and optionally elsewhere in the ring system) derivative of any one of: diethylstilboestrol, stilboestrol. When substituted, the N-substituted compounds of this invention may contain one or two N-alkyl, N-alkenyl, N-cycloallyl or N-aryl substituents, preferably containing or each containing a maximum of 10 carbon atoms. When R₁ and/or R₂ and/or R₃ and/or R₄ is alkyl, the preferred values are those where each of R₁ and R₂ and R₃ and R₄ is independently selected from lower alkyl groups containing from 1 to 6 carbon atoms, that is to say methyl, ethyl, propyl etc. When R₁ and/or R₂ and/or R₃ and/or R₄ is aryl, typical groups are phenyl and tolyl (—PhCH₃; o-, m- or p-). Where R₁ and/or R₂ and/or R₃ and/or R₄ represent cycloalkyl, typical values are cyclopropyl, cyclopentyl, cyclohexyl etc. When joined together R₃ and R₄ typically represent an alkylene group providing a chain of 4 to 6 carbon atoms, optionally interrupted by one or more hetero atoms or groups, e.g. —O— or —NH— to provide a 5-, 6- or 7-membered heterocycle, e.g. morpholino, pyrrolidino or piperidino. Within the values alkyl, cycloalkyl, alkenyl and aryl we include substituted groups containing as substituents therein one or more groups which do not interfere with the sulphatase inhibitory activity of the compound in question. Examples of non-interfering substituents include hydroxy, amino, halo, alkoxy, alkyl and aryl. Applicants have also surprisingly found that when the compound has the Formula IV where Y═—CH₂— it is not necessary for the compound to be substituted in the 2 and 4 ring positions, i.e., R₁ and R₂ may both be hydrogen. In one embodiment of this aspect, any of the ring positions (including R₁ and R₂, but excluding Y) may be substituted. Thus, according to another aspect of the present invention there is provided a sulphamate compound of the Formula X and wherein X is a sulphamate group, and Y is CH₂ and optionally any other H attached directly to the ring system is substituted by another group. X may be as described above. Any replacement for H on the ring system may be any one of the substituents described above in relation to R₁ and R₂. In an especially preferred embodiment there is no substitution on the ring system, i.e., a compound of Formula IV where Y is —CH₂— and R₁ and R₂ are both H).

FIGS. 35 to 38 show methods of preparing compounds of the present invention (See Example 15 and WO 98/24802. The sulphamate compounds of the present invention may be prepared by reacting an appropriate alcohol with a sulfamoyl chloride, R₃R₄NSO₂Cl. Preferred conditions for carrying out the reaction are as follows: Sodium hydride and a sulfamoyl chloride are added to a stirred solution of the alcohol in anhydrous dimethyl formamide at 0 C. Subsequently, the reaction is allowed to warm to room temperature whereupon stirring is continued for a further 24 hours. The reaction mixture is poured onto a cold saturated solution of sodium bicarbonate and the resulting aqueous phase is extracted with dichloromethane. The combined organic extracts are dried over anhydrous MgSO₄. Filtration followed by solvent evaporation in vacuo and co-evaporated with toluene affords a crude residue which is further purified by flash chromatography. Preferably, the alcohol is derivatised, as appropriate, prior to reaction with the sulfamoyl chloride. Where necessary, functional groups in the alcohol may be protected in known manner and the protecting group or groups removed at the end of the reaction).

FIG. 39 shows a graph illustrating the in vivo inhibition of oestrone sulphatase by NOMATE (0.1 mg/Kg/day for five days) (See Example 15 and WO 98/24802).

FIG. 40 shows a graph illustrating the lack of effect of NOMATE (0.1 mg/Kg/day for five days) on uterine weights in ovariectomised rats (See Example 15 and WO 98/24802).

DETAILED DESCRIPTION

Thus, in one aspect, the present invention provides a method of inhibiting steroid sulphatase activity in a subject in need of same, the method comprising administering to said subject a steroid sulphatase inhibiting amount of a ring system compound; which ring system compound comprises a ring to which is attached a sulphamate group of the formula

wherein each of R₁ and R₂ is independently selected from H, ally, alkenyl, cycloalkyl and aryl, or together represent allylene optionally containing one or more hetero atoms or groups in the alkylene chain; and wherein said compound is an inhibitor of an enzyme having steroid sulphatase activity (E.C.3.1.6.2); and if the sulphamate group of said compound is replaced with a sulphate group to form a sulphate compound and incubated with a steroid sulphatase enzyme (E.C.3.1.6.2) at a pH 7.4 and 37° C. it would provide a K_(m) value of less than 50 μM.

In one aspect the present invention provides, as novel compounds, the sulphamic acid esters of polycyclic alcohols, being polycyclic alcohols the sulphate of which is a substrate for enzymes having steroid sulphatase activity in accordance with the definition already provided, and their N-alkyl, N-cycloalkyl, N-alkenyl and N-aryl derivatives. These compounds are of Formula I hereinbefore given.

Preferably the polycyclic group will contain, inclusive of all substituents, a maximum of about 40 carbon atoms, more usually no more than about 30.

Preferred polycycles are those containing a steroidal ring structure, that is to say a cyclopentanophenanthrene skeleton. Preferably, the sulphamyl or substituted sulphamyl group is attached to that skeleton in the 3-position, that is to say are compounds of the Formula II:

where R₁ and R₂ are as above defined and the ring system ABCD represents a substituted or unsubstituted, saturated or unsaturated steroid nucleus, preferably oestrone or dehydroepiandrosterone.

Other suitable steroid ring systems are:

substituted oestrones, viz: 2-OH-oestrone 2-methoxy-oestrone 4-OH-oestrone 6α-OH- 7α-OH-oestrone 16α-OH-oestrone 16β-OH-oestrone oestrone oestradiols and substituted oestradiols, viz: 2-OH-17β-oestradiol 2-methoxy-17β-oestradiol 4-OH-17β- oestradiol 6α-OH-17β-oestradiol 7α-OH-17β-oestradiol 16α-OH-17α- oestradiol 16β-OH-17α-oestradiol 16β-OH-17β-oestradiol 17α-oestradiol 17β-oestradiol 17α-ethinyl-17β-oestradiol oestriols and substituted oestriols, viz: oestriol 2-OH-oestriol 2-methoxy-oestriol 4-OH-oestriol 6α-OH-oestriol 7α-OH-oestriol substituted dehydroepiandrosterones, viz: 6α-OH-dehydroepiandrosterone 7α-OH-dehydroepiandrosterone 16α-OH-dehydroepiandrosterone 16β-OH-dehydroepiandrosterone

In general terms the steroid ring system ABCD may contain a variety of non-interfering substituents. In particular, the ring system ABCD may contain one or more hydroxy, alkyl especially lower (C₁-C₆) alkyl, e.g. methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, n-pentyl and other pentyl isomers, and n-hexyl and other hexyl isomers, alkoxy especially lower (C₁-C₆) alkoxy, e.g. methoxy, ethoxy, propoxy etc., alkinyl, e.g. ethinyl, or halogen, e.g. fluoro substituents.

Suitable non-steroidal ring systems (i.e. ring system compounds) include:

diethylstilboestrol, stilboestrol and other ring systems providing sulfates having K_(m) values of less than 50 μmoles with steroid sulphatase EC3.1.6.2.

Examples of some non-steroidal ring systems are presented in the Examples section.

When substituted, the N-substituted compounds of this invention may contain one or two N-alkyl, N-alkenyl, N-cycloalkyl or N-aryl substituents, preferably containing or each containing a maximum of 10 carbon atoms. When R₁ and/or R₂ is alkyl, the preferred values are those where R₁ and R₂ are each independently selected from lower alkyl groups containing from 1 to 5 carbon atoms, that is to say methyl, ethyl, propyl etc. Preferably R₁ and R₂ are both methyl. When R₁ and/or R₂ is aryl, typical values are phenyl and tolyl (—PhCH₃; o-, m- or p-). Where R₁ and R₂ represent cycloalkyl, typical values are cyclopropyl, cyclopentyl, cyclohexyl etc. When joined together R₁ and R₂ typically represent an alkylene group providing a chain of 4 to 6 carbon atoms, optionally interrupted by one or more hetero atoms or groups, e.g. —O— or —NH— to provide a 5-, 6- or 7)-membered heterocycle, e.g. morpholino pyrrolidino or piperidino.

Within the values alkyl, cycloalkyl, alkenyl and aryl we include substituted groups containing as substituents therein one or more groups which do not interfere with the sulphatase inhibitory activity of the compound in question. Exemplary non-interfering substituents include hydroxy, amino, halo, alkoxy, alkyl and aryl.

Most preferred are compounds of the Formula III and IV:

where R₁ and R₂ are H or C₁-C₅ alkyl, i.e. oestrone-3-sulphamate and dehydroepiandrosterone-3-sulphamate and their N-(C₁-C₅) alkyl derivatives, especially the dimethyl derivatives, R₁=R₂=CH₃.

The sulphamic acid esters of this invention are prepared by reacting the polycyclic alcohol, e.g. oestrone or dehydroepiandrosterone, with a sulfamoyl chloride R₁R₂NSO₂Cl, i.e. the Reaction Scheme I.

Conditions for carrying out Reaction Scheme I are as follows:

Sodium hydride and a sulphamoyl chloride are added to a stirred solution of oestrone in anhydrous dimethyl formamide at 0° C. Subsequently, the reaction is allowed to warm to room temperature whereupon stirring is continued for a further 24 hours. The reaction mixture is poured onto a cold saturated solution of sodium bicarbonate and the resulting aqueous phase is extracted with dichloromethane. The combined organic extracts are dried over anhydrous MgSO₄. Filtration followed by solvent evaporation in vacuo and co-evaporation with toluene affords a crude residue which is further purified by flash chromatography.

Where necessary, functional groups in the polycyclic alcohol (sterol) may be protected in known manner and the protecting group or groups removed at the end of the reaction.

For pharmaceutical administration, the steroid sulphatase inhibitors of this invention can be formulated in any suitable manner utilising conventional pharmaceutical formulating techniques and pharmaceutical carriers, exipients, diluents etc. and usually for parenteral administration. Approximate effective dose rates are in the range 100 to 800 mg/day depending on the individual activities of the compounds in question and for a patient of average (70 kg) bodyweight. More usual dosage rates for the preferred and more active compounds will be in the range 200 to 800 mg/day, more preferably, 200 to 500 mg/day, most preferably from 200 to 250 mg/day. They may be given in single dose regimes, split dose regimes and/or in multiple dose regimes lasting over several days. For oral administration they may be formulated in tablets, capsules, solution or suspension containing from 100 to 500 mg of compound per unit dose. Alternatively and preferably the compounds will be formulated for parenteral administration in a suitable parenterally administrable carrier and providing single daily dosage rates in the range 200 to 800 mg, preferably 200 to 500, more preferably 200 to 250 mg. Such effective daily doses will, however, vary depending on inherent activity of the active ingredient and on the bodyweight of the patient, such variations being within the skill and judgement of the physician.

For particular applications, it is envisaged that the steroid sulphatase inhibitors of this invention may be used in combination therapies, either with another sulphatase inhibitor, or, for example, in combination with an aromatase inhibitor, such as for example, 4-hydroxyandrostenedione (4-OHA).

The invention is illustrated by the following preparative Examples and test data:

EXAMPLE 1 Preparation of Oestrone-3-sulphamate

Sodium hydride (60% dispersion; 2 eq) and sulphamoyl chloride (2 eq) were added to a stirred solution of oestrone (1 eq) in anhydrous dimethyl formamide at 0° C. Subsequently, the reaction was allowed to warm to room temperature whereupon stirring was continued for a further 24 hours.

The reaction mixture was poured onto a cold saturated solution of sodium bicarbonate and the resulting aqueous phase was extracted with dichloromethane. The combined organic extracts were dried over anhydrous MgSO₄. Filtration followed solvent evaporation in vacuo and co-evaporation with toluene afforded a crude residue which is further purified by flash chromatography.

Analysis showed the following data:

δ¹H (270 MHz; CD₃OD): 0.91 (s, 3H, C₁₈-Me), 1.40-2.55 (series of m, 13H), 2.90-2.92 (m, 2H), 7.04 (br d, 2H, J=10.44 Hz), 7.33 (br d, 1H, J=8.42 Hz). δ¹³C (67.8 MHz; CD₃OD): 14.53 (q, C₁₈-Me), 22.80 (t), 27.24 (t), 27.73 (t), 30.68 (t) 33.05 (t), 37.01 (t), 39.76 (d), 45.73 (s, C₁₈), 51.86 (d), 120.76 (d), 123.54 (d), 127.89 (d), 139.83 (s), 150.27 (s), 223.87 (s, C═O). m/z (%): 349 (9) (m⁺), 270 (100), 213 (26), 185 (43), 172 (31), 159 (21), 146 (36), 91 (33), 69 (37), 57 (73), 43 (56), 29 (24).

Microanalysis: C H N Expected: 61.87% 6.63% 4.01% Found: 61.90% 6.58% 3.95%

EXAMPLE 2 Preparation of Oestrone-3-N-methylsulphamate

The procedure of Example 1 was repeated save that sulphamoyl chloride was replaced by the same quantity of N-methylsulphamoyl chloride.

Analysis showed the following data:

δ¹H (270 MHz; CDCl₃): 0.91 (s, 3H, C₁₈-Me), 1.28-1.68 (m, 6H), 1.93-2.60 (series of m, 7H), 2.90-2.95 (m, 2H), 2.94 (d, 3H, J=5.13 Hz, MeN-), 4.68-4.71 (br m, exchangeable, 1H, —NH), 7.02-7.07 (m, 2H), 7.26-7.32 (m, 1H). m/z (%): 364 [M+H]⁺

EXAMPLE 3 Preparation of Oestrone-3-N,N-dimethylsulphamate

The procedure of Example 1 was repeated save that sulphamoyl chloride was replaced by the same quantity of N,N-dimethylsulphamoyl chloride.

Analysis showed the following data:

δ¹H (270 MHz; CDCl₃): 0.92 (s, 3H, C₁₈-Me), 1.39-1.75 (m, 5H), 1.95-2.60 (series of m, 6H), 2.82 (s, 3H, MeN-), 2.96-3.00 (m, 4H), 2.98 (s, 3H, MeN-), 7.04 (br d, 2H, J=7.69 Hz), 7.29 (br d, 1H, J=7.88 Hz). m/z (%): 377 [M]⁺

Microanalysis: C H N Expected: 63.63% 7.21% 3.71% Found: 63.50% 7.23% 3.60%

EXAMPLE 4 Inhibition of Steroid Sulphatase Activity in MCF-7 Cells by Oestrone-3-sulphamate

Steroid sulphatase is defined as: Steryl Sulphatase EC 3.1.6.2.

Steroid sulphatase activity was measured in vitro using intact MCF-7 human breast cancer cells. This hormone dependent cell line is widely used to study the control of human breast cancer cell growth. It possesses significant steroid sulphatase activity (MacIndoe et al. Endocrinology, 123, 1281-1287 (1988); Purohit & Reed, Int. J. Cancer, 50, 901-905 (1992)) and is available in the U.S.A. from the American Type Culture Collection (ATCC) and in the U.K. (e.g. from The Imperial Cancer Research Fund). Cells were maintained in Minimal Essential Medium (MEM) (Flow Laboratories, Irvine, Scotland) containing 20 mM HEPES, 5% foetal bovine serum, 2 mM glutamine, non-essential amino acids and 0.075% sodium bicarbonate. Up to 30 replicate 25 cm² tissue culture flasks were seeded with approximately 1×10⁵ cells/flask using the above medium. Cells were grown to 80% confluency and medium was changed every third day.

Intact monolayers of MCF-7 cells in triplicate 25 cm² tissue culture flasks were washed with Earle's Balanced Salt Solution (EBSS from ICN Flow, High Wycombe, U.K.) and incubated for 3-4 hours at 37° C. with 5 pmol (7×10⁵ dpm) [6,7-³H ]oestrone-3-sulphate (specific activity 60 Ci/mmol from New England Nuclear, Boston, Mass., U.S.A.) in serum-free MEM (2.5 ml) together with oestrone-3-sulphamate (11 concentrations: 0; 1 fM; 0.01 pM; 0.1 pM; 1 pM; 0.01 nM; 0.1 nM; 1 nM; 0.01 μM; 0.1 μM; 1 μM). After incubation each flask was cooled and the medium (1 ml) was pipetted into separate tubes containing [¹⁴C]oestrone (7×10³ dpm) (specific activity 97 Ci/mmol from Amersham International Radiochemical Centre, Amersham, U.K.). The mixture was shaken thoroughly for 30 seconds with toluene (5 ml). Experiments showed that >90% [¹⁴C]oestrone and <0.1% [³H]oestrone-3-sulphate was removed from the aqueous phase by this treatment. A portion (2 ml) of the organic phase was removed, evaporated and the ³H and ¹⁴C content of the residue determined by scintillation spectrometry. The mass of oestrone-3-sulphate hydrolysed was calculated from the ³H counts obtained (corrected for the volumes of the medium and organic phase used, and for recovery of [¹⁴C]oestrone added) and the specific activity of the substrate. Each batch of experiments included incubations of microsomes prepared from a sulphatase-positive human placenta (positive control) and flasks without cells (to assess apparent non-erymatic hydrolysis of the substrate). The number of cell nuclei per flask was determined using a Coulter Counter after treating the cell monolayers with Zaponin. One flask in each batch was used to assess cell membrane status and viability using the Trypan Blue exclusion method Phillips, H. J. (1973) In: Tissue culture and applications, [eds: Kruse, D. F. & Patterson, M. K.]; pp. 406-408; Academic Press, New York).

Data for oestrone-3-sulphamate are shown in Table I and FIGS. 2 and 4. Results for steroid sulphatase activity are expressed as the mean ±1 S.D. of the total product (oestrone+oestradiol) formed during the incubation period (20 hours) calculated for 10⁶ cells and, for values showing statistical significance, as a percentage reduction (inhibition) over incubations containing no oestrone-3-sulphnmate. Unpaired Student's t-test was used to test the statistical significance of results.

Oestrone-3-sulphamate (or EMATE) is a potent oestrone sulphatase (or E1-STS) inhibitor as it displays more than 99% inhibition of E1-STS activity in intact MCF-7 cells. EMATE also inhibits E1-STS in a time- and concentration-dependent manner, indicating that it acts as an active site-directed inactivator. Although EMATE inhibits E1-STS, it is possible that oestrone may be released during sulphatase inhibition, and that EMATE and its oestradiol congener may possess oestrogenic activity; thus, there can be oestrone sulphatase inhibitors that possess oestrogenic activity.

TABLE I Steroid Sulphatase Activity in MCF-7 cells in the presence of Oestrone-3-sulphamate % reduction Oestrone-3-sulphamate Steroid Sulphatase Activity over control concentration ¶ (fmol/20 hr/10⁶ cells) (% inhibition) 0 (control) 319.7 ± 18.5 — 1 fM 353.3 ± 39.0 — 0.01 pM 362.3 ± 21.2 — 0.1 pM 330.7 ± 17.8 — 1 pM 321.8 ± 6.2 — 0.01 nM 265.1 ± 11.0* 17.2% 0.1 nM 124.8 ± 12.4*** 60.9% 1 nM 16.49 ± 4.7*** 95.0% 0.01 μM  3.92 ± 0.4*** 98.8% 0.1 μM  2.53 ± 1.1*** 99.2% 1 μM  1.68 ± 0.7*** 99.5% ¶ mean ± 1 S.D. n = 3 *p ≦ 0.05 ***p ≦ 0.001

EXAMPLE 5 Inhibition of Steroid Sulphatase Activity in MCF-7 Cells by Oestrone-3-N,N-dimethylsulphamate

An identical experimental protocol to that described in Example 4 was used to generate results for oestrone-3-N,N-dimethylsulphamate except that incubations contained oestrone-3-N,N-dimethylsulphamate (5 concentrations: 0; 0.001 μM; 0.01 μM; 0.1 μM; 1 μM) in place of oestrone-3-sulphamate.

Results for oestrone-3-N,N-dimethysulphamate are shown in Table II and FIG. 3 and are expressed in an identical manner to Table I and FIG. 2 respectively. Additionally the log dose-response curve is compared with oestrone-3-sulphamate in FIG. 4.

TABLE II Steroid Sulphatase Activity in MCF-7 cells in the presence of Oestrone-3-N,N-dimethylsulphamate Oestrone-3-N,N- Steroid Sulphatase % reduction dimethylsulphamate Activity ¶ over control concentration (fmol/20 hr/10⁶ cells) (% inhibition) 0 (control) 82.63 ± 3.6 — 0.001 μM 68.33 ± 3.2** 17.3% 0.01 μM  46.0 ± 4.9*** 44.3% 0.1 μM 17.43 ± 4.3*** 78.9% 1 μM 11.89 ± 3.7*** 85.6% ¶ mean ± 1 S.D. n = 3 **p ≦ 0.01 ***p ≦ 0.001

EXAMPLE 6 Inhibition of Steroid Sulphatase Activity in MCF-7 Cells by Pre-treatment with Oestrone-3-N,N-dimethylsulphamate and Oestrone-3-N,N-dimethylsulphamate

A similar experimental protocol to that described in Example 4 was used to determine the effect of pre-treating MCF-7 cells with oestrone-3-sulphamate and oestrone-3-N,N-dimethylsulphamate respectively.

Intact monolayers were initially incubated for 2 hours at 37° C. with 0.1 μM oestrone-3-sulphamate, oestrone-3-N,N-dimethylsulphamate or medium alone (control). The medium bathing the cells was then removed by aspiration and cells were washed 3 times successively with 5 ml of medium on each occasion. The resultant ‘washed’ cells were then re-suspended and incubated for 34 hours at 37° C. in medium containing 5 pmol (7×10⁵ dpm) [6,7-³H]oestrone-3-sulphate. All other aspects were identical to those described in Examples 3 and 4.

Results for oestrone-3-sulphamate and oestrone-3-N,N-dimethylsulphamate are shown in Table III and are expressed in a similar manner to Table I.

TABLE III Steroid Sulphatase Activity in MCF-7 cells pre-incubated with Oestrone-3-sulphamates Steroid Sulphatase % reduction over Activity ¶ (fmol/20 control (% Pre-treatment hr/10⁶ cells) inhibition) Control 65.4 ± 6.4 — Oestrone-3-sulphamate  1.7 ± 0.2*** 97.4% Oestrone-3-N,N- 53.1 ± 3.4* 18.8% dimethylsulphamate ¶ mean ± 1 S.D. n = 3 *p ≦ 0.05 ***p ≦ 0.001

EXAMPLE 7 Inhibition of Steroid Sulphatase Activity in Placental Microsomes by Oestrone-3-sulphamate

Sulphatase-positive human placenta from normal term pregnancies (Obstetric Ward, St. Mary's Hospital, London) were thoroughly minced with scissors and washed once with cold phosphate buffer (pH 7.4, 50 mM) then re-suspended in cold phosphate buffer (5 ml/g tissue). Homogenisation was accomplished with an Ultra-Turrax homogeniser, using three 10 second bursts separated by 2 minute cooling periods in ice. Nuclei and cell debris were removed by centrifuging (4° C.) at 2000 g for 30 minutes and portions (2 ml) of the supernatant were stored at −20° C. The protein concentration of the supernatants was determined by the method of Bradford (Anal. Biochem., 72, 248-254 (1976)).

Incubations (1 ml) were carried out using a protein concentration of 100 μg/ml, substrate concentration of 20 μM [6,7-³H]oestrone-3-sulphate (specific activity 60 Ci/mmol from New England Nuclear, Boston, Mass., U.S.A.) and an incubation time of 20 minutes at 37° C. Eight concentrations of oestrone-3-sulphamate were employed: 0 (i.e. control); 0.05 μM; 0.1 μM; 0.2 μM; 0.4 μM; 0.6 μM; 0.8 μM; 1.0 μM. After incubation each sample was cooled and the medium (1 ml) was pipetted into separate tubes containing [¹⁴C]oestrone (7×10³ dpm) (specific activity 97 Ci/mmol from Amersham International Radiochemical Centre, Amersham, U.K.). The mixture was shaken thoroughly for 30 seconds with toluene (5 ml). Experiments showed that >90% [¹⁴C]oestrone and <0.1% [³H]oestrone-3-sulphate was removed from the aqueous phase by this treatment. A portion (2 ml) of the organic phase was removed, evaporated and the ³H and ¹⁴C content of the residue determined by scintillation spectrometry. The mass of oestrone-3-sulphate hydrolysed was calculated from the ³H counts obtained (corrected for the volumes of the medium and organic phase used, and for recovery of [¹⁴C]oestrone added) and the specific activity of the substrate.

Results for oestrone-3-sulphamate are shown in Table IV and FIG. 5. Results for steroid sulphatase activity are expressed in Table IV as total product (oestrone+oestradiol) formed during the incubation period (time) and as a percentage reduction (inhibition) over incubations containing no oestrone-3-sulphamate which acted as control. Results for steroid sulphatase activity are expressed in FIG. 4 as percentage reduction (inhibition) over control against concentration of oestrone-3-sulphamate and include the calculated IC₅₀ value (i.e. the concentration of oestrone-3-sulphamate which produces 50% inhibition in relation to control) of 0.07 μM.

TABLE IV Steroid Sulphatase Activity in placental microsomes in the presence of Oestrone-3-sulphamate Oestrone-3- % reduction sulphamate Steroid Sulphatase Activity ¶ over control concentration (pmol/hr/0.1 mg protein) (% inhibition) 0 (control) 768.6 — 0.05 μM 430.4 44.0% 0.1 μM 305.9 60.2% 0.2 μM 140.0 81.8% 0.4 μM 83.3 89.2% 0.6 μM 61.8 92.0% 0.8 μM 49.2 93.6% 1.0 μM 51.6 93.3% ¶ mean of 2 estimates

EXAMPLE 8 Inhibition of Steroid Sulphatase Activity in Liver Microsome Preparations from Rats Treated with Subcutaneous Oestrone-3-sulphamate

Four groups of 3 female Wistar rats (weight range 80-110 g) were given 100 ml subcutaneous injections (once daily for 7 days, vehicle: propylene glycol) of either:

-   -   Propylene glycol (vehicle control)     -   Oestrone-3-sulphamate (10 mg/kg/day)     -   Oestrone-3-sulphate (10 mg/kg/day) (substrate control)     -   Oestrone-3-sulphate (10 mg/kg/day)+Oestrone-3-sulphate (10         mg/kg/day).

On the eighth day all rats were sacrificed and livers were removed by dissection. Liver microsomal preparations were prepared by an identical protocol to that describe in Example 6 except that the tissue source was rat liver and that duplicate experiments to determine steroid sulphatase activity were performed using [6,7H]oestrone-3-sulphate and [7-³H]dehydroepiandrosterone-3-sulphate as separate substrates.

Results for steroid sulphatase activity are shown in Table V arid are expressed as total product formed during the incubation period in the form of mean ±1 S.D. Results for incubations of tissue obtained from groups of rats treated with oestrone-3-sulphamate are also expressed as a percentage reduction (inhibition) in steroid sulphatase activity compared to their respective controls.

TABLE V Steroid Sulphatase Activity in Liver Microsome Preparations from Rats treated with subcutaneous Oestrone-3-sulphamate Steroid Sulphatase Assay Activity ¶ (nmol/30 % reduction Treatment Group Substrate min/200 mg protein) over control control (vehicle) E₁-S 20.95 ± 0.2 — E₁-SO₃NH₂ E₁-S  0.34 ± 0.1*** 98.4% control (E₁-S) E₁-S  20.6 ± 0.4 — E₁-S + E₁-SO₃NH₂ E₁-S  0.21 ± 0.03*** 99.0% control (vehicle) DHA-S  1.73 ± 0.4 — E₁-SO₃NH₂ DHA-S  0.1 ± 0.01*** 94.2% control (E₁-S) DHA-S  1.71 ± 0.1 — E₁-S + E₁-SO₃NH₂ DHA-S  0.09 ± 0.01*** 94.7% ¶ mean ± 1 S.D. n = 3 ***≦ 0.001 E₁-S = oestrone-3-sulphamate DHA-S = dehydroepiandrosterone-3-sulphate E₁-SO₃NH₂ = oestrone-3-N,N-dimethylsulphamate

EXAMPLE 9

Starting with the appropriate parent compound, the ring system sulphamates according to the present invention were prepared essentially as follows. In this regard, a solution of the appropriate parent compound in anhydrous DMF was treated with sodium hydride [60% dispersion; 1.2 equiv.] at 0° C. under an atmosphere of N₂. After evolution of hydrogen had ceased, sulfamoyl chloride in toluene [excess, ca. 5 equiv.] was added and the reaction mixture was poured into brine after warming to room temperature overnight and diluting with ethyl acetate. The organic fraction was washed exhaustively with brine, dried (MgSO₄), filtered and evaporated. The crude product obtained was purified by flash chromatography and recrystallisation to give the corresponding sulfamate. All the compounds were fully characterized by spectroscopic and combustion analysis.

Example compounds are as follows:

EXAMPLE 9a 4-n-Heptyl phenyl-O-sulphamate (9a)

4-n-Heptyloxyphenol (1.0 g, 4.80 mmol) gave a crude product (1.41 g) which was fractionated on silica (200 g) with chloroform/acetone (8:1), and upon evaporation the second fraction gave a pale white residue (757 mg) which was recrystallized from acetone/hexane (1:5) to give 9a as white crystals (0.557 g).

Analytical results were as follows:

m.p. >42° C. (dec.) R_(f)s=0.56, 0.69 and 0.8 for chloroformlacetone 8:1, 4:1 and 2:1 respectively νmax (KBr) 3440, 3320 (—NH₂), 1370 (—SO₂N—) cm⁻¹ δ_(H) (acetone-d₆) (270 MHz) 0.89 (3H, t, C-4-CH ₃), 1.34 (8H, m, —(CH ₂)₄CH₃), 1.79 (2H, pentet, —CH ₂(CH₂)₄CH₃), 4.0 (2H, t, J=6.4 Hz, —OCH ₂—), 6.95 (2H, dd, J_(C-3-H and C-5-H)=2.2 Hz and J_(C-3-H and C-2-H)=6.97 Hz, C-3-H and C-5-H), 7.01 (2H, br s, exchanged with D₂O,—OSO₂NH ₂), 7.23 (2H, dd, J_(C-2-H and C-6-H)=2.4 Hz and J_(C-2-H and C-6-H)=6.97 Hz, C-2-H and C6-H) MS: m/z (+ve ion FAB in m-NBA, rel. intensity) 287.1 [100, (M)⁺], 208.2 [30, (M—SO₂NH₂)⁺ MS: m/z (−ve ion FAB in m-NBA, rel. intensity) 286.0 [100, (M−H)], 96.0 (10) and 77.9 (20). Acc. MS: m/z (FAB)⁺ 288.1246 C₁₃H₂₂NO₄S requires 288.1269. Found C, 54.2; H, 7.35; N, 4.7; C₁₃H₂₁NO₄S requires C, 54.33; H, 7.37; N, 4.87%.

Biological Data:

-   % Inhibition in MCF-7 Cells at 10 μM=99±2 -   % Inhibition in Placental Microsomes at 10 μM=40±2 -   % Inhibition in vivo from a single dose of 10 mg/kg=22±3

EXAMPLE 9(b) (E) Methyl-γ-methyl-6-nonenamide-N-(3-methoxyphenyl4-O-sulphamate) (9b)

E-Capsaicin ((E)-N-(4-Hydroxy-3-methoxyphenyl)-methyl-γ-methyl-6-nonenamide) (100 mg, 0.3274 mmol) gave a beige crude product (130 mg) which was fractionated on silica (100 g) with chloroform/acetone (2:1), and upon evaporation the second fraction gave a pale white residue (85 mg) which was recrystallized from acetone/hexane (1:2) to give 9b as pale white crystals (63 mg, 50%).

Analytical results were as follows: m.p=114-116° C. R_(f)s=0.4 and 0.15 for chloroform/acetone 2:1 and 4:1 respectively νmax (KBr) 3490,3300 (—NH₂), 1650 (CO), 1380 (—SO₂N—) cm⁻¹ δ_(H) (CDCl₃) (270 MHz) 0.94 (6H, d, J=6.6 Hz, 2x-CH ₃), 1.4 (2H, pentet, —COCH₂CH₂— or —CH₂CH₂CH═CH—), 1.62 (2H, pentet, —CH₂CH₂CH═CH— or —COCH₂CH₂—), 2.0 (2H, q, —CH ₂CH═CH—), 2.2 (3H, t, —CH ₂CONH— and —CH(CH₃)₂), 3.87(3H, s, C-3-OCH ₃), 4.39 (2H, d, J=5.86 Hz, ArCH ₂NHCO), 5.14 (2H, br s, exchanged with D₂O, —OSO₂NH ₂), 5.34 (2H, m, —CH═CH—), 5.87 (1H, t, —NHCO—), 6.84 (1H, dd, J=_(C-6-H and C-2-H) 1.92 Hz and J=_(C-6-H and C-5-H) 8.15 Hz C-6-H), 6.86 (1H, d, J=_(C-1-H and C-6-H) 1.83 Hz, C-1-H) and 7.26 (1H, d, J=_(C-5-H and C-6-H) 8.08 Hz, C-5-H). MS: m/z (+ve ion FAB in m-NBA, rel. intensity) 385.2 [100, (M+H)⁺], 304.2 (20), 287.1 (10) MS: m/z (−ve ion FAB in m-NBA, rel. intensity) 383.1 [100, (M−H)⁻], 302.2 (10), 95.9 (10) and 77.9 (35) Found C, 56.2; H, 7.38; N, 7.29; C₁₈H₂₈N₂O₅S requires C, 56.23; H, 7.34; N, 7.29%.

Biological Data:

-   % Inhibition in MCF-7 Cells at 10 μM=99±2 -   % Inhibition in Placental Microsomes at 10 μM=40±2 -   % Inhibition in vivo from a single dose of 10 mg/kg=22±3

9(c) 2-Nitrophenol-O-sulfamate (9c)

A stirred solution of 2-nitrophenol (1.391 g, 10.0 mmol) in anhydrous DMF (20 mL) was treated with sodium hydride (60% dispersion, 400 mg, 10.0 mmol) at 0° C. under an atmosphere of N₂. After evolution of hydrogen had ceased, sulfamoyl chloride (2 eq.) was added. The reaction mixture was stirred at room temperature overnight and then poured into water (150 mL). The resulting mixture was extracted with ethyl acetate (150 mL) and the organic portion separated was washed with brine (5×100 mL), dried (MgSO₄), filtered and evaporated in vacuo at 40° C. Purification by flash chromatography (ethyl acetate/hexane, 1:1) gave the crude 2-nitrophenol-O-sulfamate which was further purified by recrystallization from hot chloroform to afford the title compound as white crystals (333 mg, 745.8 μmol). The residue recovered, from the evaporation of the mother liquor, was recrystallized from chloroform/hexane to give further crops of the title compound (a total of 252 mg, 564.4 μmol, 26% overall).

Analytical results were as follows:

mp 102-103° C. ¹H NMR (270 MHz, CDCl₃) δ 5.29 (2H, br s, exchanged with D₂O, OSO₂NH₂), 7.48 (1H, m, C4-H or C5-H), 7.66 (1H, dd, J=1.5 and 8.3 Hz, C3-H or C6-H), 7.71 (1H, m, C4H or C5-H) and 8.05 (1H, dd, J=1.5 and 8.3 Hz, C3-H or C6-H) MS (EI, 70 eV) m/z (rel. intensity) 218(2, M⁺), 139[100, (M-SO₂NH)⁺]; MS (CI, isobutane) m/z (rel. intensity) 219[27, (M+H)⁺], 202[10, (M+H—NH₃)⁺], 140[100, (M+H—SO₂NH)⁺], 122(15, (M-OSO₂NH₂)⁺]. Anal. (C₆H₆N₂O₅S) C, H, N.

Biological Data:

-   % Inhibition in MCF-7 Cells at 10 μM=99±2 -   % Inhibition in Placental Microsomes at 10 μM=40±2 -   % Inhibition in vivo from a single dose of 10 mg/kg=22±3

EXAMPLE 10

Starting with the appropriate phenolic parent compound (if there are two phenol groups, it may be necessary to protect one of them using standard protection techniques for at least a part of the reaction), the ring system sulphamates according to the present invention are prepared essentially as follows. Likewise, a solution of the appropriate parent compound in anhydrous DMF is treated with sodium hydride [60% dispersion; 1.2 equiv.] at 0° C. under an atmosphere of N₂. After evolution of hydrogen has ceased, sulfamoyl chloride in toluene [excess, ca. 5 equiv.] is added and the reaction mixture is poured into brine after warming to room temperature overnight and diluting with ethyl acetate. The organic fraction is washed exhaustively with brine, dried (MgSO₄), filtered and evaporated. The crude product obtained is purified by flash chromatography and recrystallisation to give the corresponding sulfamate. All the compounds are fully characterized by spectroscopic and combustion analysis.

The following compounds of the present invention are made and are found to be steroid sulphatase inhibitors in accordance with the present invention.

Example 11

Starting with the appropriate phenolic parent compound (if there are two phenol groups, it may be necessary to protect one of them using standard protection techniques for at least a part of the reaction), the ring system sulphamates according to the present invention are prepared essentially as follows. Here, a solution of the appropriate parent compound in anhydrous DMF is treated with sodium hydride [60% dispersion; 1.2 equiv.] at 0° C. under an atmosphere of N₂. After evolution of hydrogen has ceased, N-methyl sulfamoyl chloride in toluene [excess, ca. 5 equiv.] is added and the reaction is mixture is poured into brine after warming to room temperature overnight and diluting with ethyl acetate. The organic fraction is washed exhaustively with brine, dried (MgSO₄), filtered and evaporated. The crude product obtained is purified by flash chromatography and recrystallisation to give the corresponding sulfamate. All the compounds are fully characterized by spectroscopic and combustion analysis.

The following compounds of the present invention are made and are found to be steroid sulphatase inhibitors in accordance with the present invention. (In the following formulae, the methyl and H groups on the sulphamate group can be interchanged.)

Example 12

Starting with the appropriate phenolic parent compound (if there are two phenol groups, it may be necessary to protect one of them using standard protection techniques for at least a part of the reaction), the ring system sulphamates according to the present invention are prepared essentially as follows. Here, a solution of the appropriate parent compound in anhydrous DMF is treated with sodium hydride [60% dispersion; 1.2 equiv.] at 0° C. under an atmosphere of N₂. After evolution of hydrogen has ceased, N, N-dimethyl sulfamoyl chloride in toluene [excess, ca. 5 equiv.] is added and the reaction mixture is poured into brine after warming to room temperature overnight and diluting with ethyl acetate. The organic fraction is washed exhaustively with brine, dried MgSO₄), filtered and evaporated. The crude product obtained is purified by flash chromatography and recrystallisation to give the corresponding sulfamate. All the compounds are fully characterized by spectroscopic and combustion analysis.

The following compounds of the present invention are made and are found to be steroid sulphatase inhibitors in accordance with the present invention.

EXAMPLE 13

The compounds of the present invention may be, prepared by a process that comprises a Packman synthesis step. Packman synthesis is known in the art.

Sulphamoylation of Coumarins

The general procedure for the sulphamoylation of coumarins was as follows. A solution of an appropriate coumarin in anhydrous DMF (ca. 40 ml per g of coumarin) was treated with sodium hydride [60% dispersion; 1 equiv] at 0° C. under an atmosphere of N₂. After evolution of hydrogen had ceased, sulphamoyl chloride in toluene [ca. 0.68 M, 1.5 equiv] was added and the reaction mixture was poured into water after warming to room temperature overnight and then the crude product was then quenched. The organic fraction in ethyl acetate (150 ml) was washed exhaustively with brine, dried (MgSO₄), filtered and evaporated. The crude product obtained was purified by flash chromatography followed by recrystallisation to give the corresponding sulphamate. All new compounds were fully characterised by spectroscopic and combustion analysis. The synthesis of 4 methylcoumarin-7-O-sulphamate (14) is shown in FIG. 9.

Following this general procedure, compounds 13-16 (as shown in FIG. 7)—i.e. coumarin-7-O-sulphamate (13), 4-methylcoumarin-7-O-sulphamate (14), 3,4,8-trimethylcoumarin-7-O-sulphamate (15) and 4-(trifluoromethylcoumarin)-7-O-sulphamate (16)—were prepared. More details on the synthesis of these compounds now follow.

The synthesis of compound 12 (as shown in FIG. 7) is also discussed below.

Preparation of Coumarin-7-O-sulphamate (13)

Following the above-mentioned general procedure, 7-Hydroxycoumarin (500 mg, 3.082 mmol) gave a crude product (605 mg) which was fractionated on silica (200 g) by gradient elution with chloroform/acetone (8:1, 500 ml; 4:1, 1000 ml and then 2:1, 500 ml). Upon evaporation, the second fraction gave a creamy yellow residue (389 mg, 52.3%) which was rectystallised in ethyl acetate/hexane (1:1) to give (13) as dull white crystals (239 mg).

Analytical data were as follows:

M.p. 170.0-171.5° C.; R_(f)s=0.48 (ether), 0.67 (ethyl acetate), 0.19 (chloroform/acetone, 4:1); νmax (KBr) 3360, 3210, 3060, 1720, 1615, 1370, 1125 cm⁻¹; δ_(H) (DMSO-d₆/CDCl₃, Ca. 1:25) 6.415 (1H, d, J_(C-4-H,C-3-H)=9.7 Hz, C-3-H), 7.285 (1H, dd, J_(C-8-H,C-6-H)=2.3 Hz and J_(C-5-H,C-6-H)=8.5 Hz, C-6-H), 7.379 (1H, d, J_(C-6-H,C-8-H)=2.2 Hz, C-8-H), 7.508 (2H, br s, D₂O exchanged, —NH ₂), 7.543 (1H, d, J_(C-6-H,C-5-H)=8.4 Hz, C-5-H) and 7.760 (1H, d, J_(C-3-H,C-4-H)=9.7 Hz, C-4-H). MS: m/z (E.I., rel. intensity) 241.0(10), 162.0(97), 134.0(100), 105.0(23). Acc. MS: m/z 241.0068, C₉H₇NO₅S requires 241.0045. Found: C, 44.8; H. 2.89; N, 5.82. C₉H₇NO₅S requires C, 44.81; H, 2.92; N, 5.81%.

Preparation of 4-Methylcoumarin-7-O-sulphamate (14)

Following the above-mentioned general procedure, 7-Hydroxymethylcoumarin (500 mg, 2.753 mmol) gave a crude product (633 mg) which was fractionated on silica (200 g) by gradient elution with chloroformlacetone (8:1, 500 ml; 4:1, 1000 ml, 2:1, 500 ml and then 1:1, 500 ml). Upon evaporation, the second fraction gave a creamy yellow residue (425 mg, 60.5%) which was recrystallised in acetonetchloroform (3:5) to give (14) as colorless rhombic crystals (281 mg).

Analytical data were as follows:

M.p. 165-167° C.; R_(f)s=0.48 (ether), 0.29 (ether/hexane 8:1), 0.26 (chloroform/acetone, 4:1); ν_(max) (KBr) 3320, 3180, 3080, 1700, 1620, 1560, 1380, 1125 cm⁻¹; δ_(H) (acetone-d₆) 2.507 (3H, s, —CH ₃), 6.339 (1H, s, C-3-H), 7.299 (2H, d, m, C-6-H and C-8-H), 7.390 (2H, br s, D₂O exchanged, —NH ₂ and 7.850 (1H, d, J_(C-6-H,C-5-H)=9 Hz, C-5-H). MS: m/z (+ve ion FAB in m-NBA, rel. intensity) 542.2(15), 511.1[45, (2M+H)⁺], 461.2(20), 409.1[60, (M+H+NBA)⁺], 393.3[60, (M+H+NBA-16)⁺], 329.2[10, (M+H+NBA-80)⁺], 256.1 [100, (M+H)⁺]. MS: m/z (−ve ion FAB in m-NBA, rel. intensity) 421.0(20), 407.1[15, (M−H+NBA)⁻], 335.1(14), 254[100, (M−H)⁻], 175.1[32, (M−H-79)⁻], 121.0(17). Found: C, 47.2; H, 3.56; N, 5.51. C₁₀H₉NO₅S requires C, 47.06; H, 3.55; N, 5.49%.

Preparation of 3,4,8-Trimethylcoumarin-7-O-sulphamate (15)

Following the above-mentioned general procedure, 7-Hydroxy-3,4,8-trimethylcoumarin (1.0 g, 4.896 mmol) gave a crude product (1.33 g) which upon recrystallisation in hot ethyl acetate yielded 238 mg of starting coumarin. The mother liquor was evaporated and the white residue obtained (1.13 g) was fractionated on silica (200 g) with ether. The second fraction was collected, evaporated and the residue obtained (519 mg, 37.4%) was recrystallised in acetonethexane (1:2) to give (15) as pale yellow crystals (312 mg).

Analytical data were as follows:

M.p. 197-202° C.; R_(f)s=0.50 (ether), 0.69 (ethyl acetate); νmax (KBr) 3310, 3040, 1680, 1600 cm⁻¹; δ_(H) (acetone-d₆) 2.176, 2.383 and 2.458 (9H, three s, 3×CH ₃), 7.374 (1H, d, J_(C-5-H,C-6-H)=8.8 Hz, C-6-H), 7.390 (2H, br s, D₂O exchanged, —NH ₂) and 7.682 (1H, d, J_(C-6-H,C-5-H)=8.8 Hz, C-5-H). MS: m/z (E.I., rel. intensity) 283.1(10), 204.1(45), 176.1(40), 161.1(22), 69.1(56), 57.1(40), 43.1(100). Acc. MS: m/z 283.0497. C₁₂H₁₃NO₅S requires 283.0514. Found: C, 50.86; H, 4.63; N, 4.97. C₁₂H₁₃NO₅S requires C, 50.88; H, 4.63; N, 4.94%.

Preparation of 4-(Trifluoromethyl)coumarin-7-O-sulphamate (16)

Following the above-mentioned general procedure, 7Hydroxy-4-(trifluoromethyl)-coumarin (0.90 g. 3.911 mmol) gave a crude product (1.20 g) which was fractionated on silica (200 g) with ether/chloroform (1:4). The residue (392 mg) from the third fraction was further purified by fractionating on silica (100 g) with ether. The first fraction then collected gave a residue (295 mg, 24.4%) which upon recrystallised in ethyl acetatethexane (1:3) gave (16) as white needle-shaped crystals (160 mg).

Analytical data were as follows:

M.p. 165-168° C. R_(f)s=0.67 (ether), 0.24 (ether/chloroform, 1:4); νmax (KBr) 3360, 3240, 3100, 1720, 1620, 1380, 1160 cm⁻¹; δ_(H) (acetone-d₆) 6.995 (1H, s, C-3-H), 7.461 (1H, dd, J_(C-8-H,C-6-H)=2.8 Hz and J_(C-5-H,C-6-H)=8.1 Hz, C-6-H), 7.478 (1H, s, C-8-H), 7.53 (2H, br s, D₂O exchanged, —NH ₂) and 7.89 (1H, m, C-5-H). ¹H-NMR spectrum of (16) in DMSO-d₆/CDCl₃ (ca. 1:15) showed partial decomposition to the starting coumarin. MS: m/z (E.I., rel. intensity) 309.0(2.6), 230.0(77), 202.0(100), 183.5(5), 173.0(10), 69.0(33). Acc. MS: m/z 308.9874, C₁₀H₆F₃NO₅S requires 308.9919. Found: C, 38.8; H, 1.85; N, 4.53. C₁₀H₆F₃NO₅S requires C, 38.84; H, 1.96; N. 4.53%.

Preparation of 7-(Sulphoxy)4-Methylcoumarin, sodium salt (12)

To a solution of 7-hydroxy4-metlylcoumarin (1.0 g, 5.676 mmol) in dried pyridine (20 ml) under an atmosphere of N₂ [FIG. 8] was added sulphur trioxide-pyridine complex (1.8 g, 11.35 mmol, 2 equiv.) and the reaction mixture was stirred overnight. After removal of pyridine, methanol (20 ml) was added to the creamy syrup obtained and the resulting light yellow solution was basified (pH˜8) by dropwise addition of sodium hydroxide in methanol (1 M, ca. 18 ml). The bright yellow suspension formed was filtered and the precipitated washed with more methanol. The filtrate was then concentrated to 30-40 ml and ether (total 120 ml) was added in portions until precipitation completed. The light beige precipitate was collected (711 mg) and 582 mg of which was recrystallised in methanol/ether (1:1) to give (12) as light creamy yellow crystals (335 mg).

Analytical data were as follows:

M.p. 172-175° C. (dec.); R_(f)s=0.51 (methanol/ethyl acetate, 1:3), 0.67 (methanol/ether, 1:3); νmax (KBr) 3500 (br), 3080, 1680, 1610, 1560, 1300, 1260, 1050 cm⁻¹; δ_(H) (DMSO-d₆) 2.407 (3H, s, —CH ₃), 6.269 (1H, s, C-3-H), 7.20 (2H, m, C-6H and C-8-H and 7.695 (1H, d, J_(C-6-H,C-5-H)=8.8 Hz, C-5-H). MS: m/z (+ve ion FAB in m-NBA, rel. intensity) 176(100, NBA+Na⁺). MS: m/z (−ve ion FAB in m-NBA. rel. intensity) 175.1 (14, M-Na⁺—SO₃), 255.0 (100, M-Na⁺). 408.0 (8, M-Na⁺+NBA), 431.0 (15, M+153), 444.0(20), 533.0(15), 230.0(77), 202.0(100), 183.5(5), 173.0(10), 69.0(33). Acc. MS: m/z (-ve ion FAB in glycerol, rel. intensity) 254.9982(25), C₁₀H₇O₆S requires 254.9963. Found: C, 40.3; H, 2.92. C₁₀H₇O₆NaS.H₂O requires C, 40.55; H, 3.06%. HPLC [Spherisorb ODS5, 25×4.6 mm; Mobile phase: MeOH/H₂O (70:30), Flow rate: 1 ml/min; λ_(max): 316 nm]: t_(R)=1.5 min. c.f. 7-hydroxy-4-methylcoumarin, 3.6 min.

Other data were as follows:

Compound 12 is stable in bases such as sodium hydroxide in methanol but not in acidic conditions. In addition, incomplete basification of the reaction mixture with sodium hydroxide in methanol (<3 equivalents) leads to decomposition of (12). Two equivalents of sodium hydroxide are required for consuming excess sulphur trioxide-pyridine complex to yield the neutral sodium sulphate. Insufficient amount of sodium hydroxide will therefore lead to the formation of sodium hydrogen sulphate which is acidic. Compound 12 appears labile to high temperature as one experiment has shown complete decomposition to 7-hydroxy-4-methylcoumarin after heating (12) as solid at 90° C. for 4 h.

In Vitro Tests

The above-mentioned coumarin sulphamates were tested for their ability to inhibit E1-STS activity using intact MCF-7 breast cancer cells or placental microsomes (100,000 g fraction) essentially as previously described.

To examine whether compound (12) could act as a substrate for E1-STS, 100 μg of the compound was incubated for 1 hour with placental microsomes in the absence or presence of EMATE (10 μM). The unconjugated coumarin formed at the end of the incubation was extracted with diethyl ether. After evaporation of solvent, the residue was examined by TLC using ethyl acetatelmethanol (80:20) as eluent, in which the coumarin sulphate (12) and 7-hydroxy-4methylcoumarin had R_(f) values of 0.79 and 0.95 respectively. Only unconjugated 7-hydroxy-4-methylcoumarin was detected after incubation of compound (12) with placental microsomes. The inclusion of EMATE in the reaction mixture reduced the hydrolysis of compound (12) by E1-STS, indicating that the coumarin sulphate is indeed a substrate for the sulphatase.

The dose-dependent inhibition of oestrone sulphatase in intact MCF-7 beast cancer cells by coumarin-7-O-sulphamate (13), 4-methylcoumarin-7-O-sulphamate (14), 3,4,8-trimethyl-coumarin-7-O-sulphamate (15) and 4-(trifluoromethyl)coumarin-7-O-sulphamate (16) can be seen from FIG. 10. Assays were performed essentially as previously described. Monolayers of intact MCF-7 cells in 25 cm³ flasks were incubated for 20 h at 37° C. with [³H]oestrone sulphate (2 nM) and coumarin sulphamates at 0.1-10 μM. Oestrone sulphatase activity was determined by measuring the total amount of ³H-labeled oestrone and oestradiol formed. Sulphatase activity in untreated cells was 100-200 fmol/20 h/10⁶ cells. Each point represents the mean ±s.d. of triplicate measurements. (J. Med. Chem. 1994, 37, 219-21; Biochemistry 1995, 34, 11508-14.)

The free parent coumarins of all coumarin sulphamates prepared showed little or no E1-STS inhibitory activity when tested up to 10 μM. However. in contrast, all four coumarin sulphamates (compounds 13-16) inhibited oestrone sulphatase inhibitory activity in a dose-dependent manner (FIG. 10) and the inhibition at 10 μM ranged from 71.5% for compound 16 to 93.3% for compound 14. The IC₅₀ for inhibition of E1-STS by compound 14, the most effective inhibitor, measured using intact MCF-7 cells was 380 nM.

The time- and concentration-dependent inactivation of oestrone sulphatase by 4-methyl-coumarin-7-O-sulphamate (14) can be seen from FIG. 11. Placental microsomes (200 μg) were preincubated with (14) (control, ●; 0.5 μM, Δ and 10 μM, *) for 0-30 min at 37° C. followed by incubation with dextrancharcoal for 10 min at 4° C. Dextran-charcoal was sedimented by centrifugation and portions of the supernatants were then incubated with [³H]oestrone sulphate (20 μM) for 1 h at 37° C. to assess remaining sulphatase activity. Duplicate experiments were run at each concentration, but assays for residual activity were taken at different times in each experiment.

As with EMATE, compound 14 inhibited E1-STS activity in a time- and concentration-dependent manner in a biphasic fashion (FIG. 11), indicating a similar mechanism of action (potential chemical modification of two active site residues). At 10 μM, compound 14 reduced the original E1-STS activity by 95% after preincubating the enzyme with the inhibitor for 20 min.

Additional experiments revealed that compound 14 inhibited placental microsomal DHA-STS activity by 93.6% at the same concentration.

In Vivo Tests

In order to examine if compound 14 possessed oestrogenic activity and also to test its ability to inhibit E1-STS in vivo, it was administered to rats (1 mg/kg subcutaneously, in propylene glycol for 5 days) 14 days after ovariectomy had been performed.

Administration of compound 14 did not result in any significant increase in the uterine weight in these rats (data not shown), showing that compound 14 showed reduced oestrogenic agonist properties. The E1-STS activity in the uteri obtained from these animals was inhibited by 89.4% compared with the activity in untreated animals.

Preliminary data also demonstrate potent oral activity in rats for compound 14, similar to that observed for EMATE.

In addition to these in vivo results, another series of rats (each weighing approximately 200 g) received 4-methyl coumarin-7-O-sulphamate (compound 14) orally in propylene glycol either as a single dose (SD) or daily for seven days (Multiple Dose, MD).

Inhibition of sulphatase activity was assessed in white blood cells (wbcs) that were collected after a SD or MD. Sulphatase activity was assayed using labelled oestrone sulphate as the substrate and measuring the release of oestrone.

The results are shown in FIG. 12 and in the Table below:

% Inhibition Dose mg/kg SD MD 0.1 72 65 1.0 85 85 10.0 96 89

Similar results were found with liver cells.

Compound 14 (coumate) therefore demonstrates potent oral activity.

Other modifications of the present invention will be apparent to those skilled in the art.

EXAMPLE 14 Compounds Synthesised

The following sulphamate derivatives were synthesised from the following parent compounds:

PARENT SULPHAMATE COMPOUND COMPOUND 1 2 3 4 5 6 7 8 9 10  wherein

-   1=6-hydroxy flavone -   2=flavone-6-sulphamate -   3=7-hydroxy flavone -   4=flavone-7-sulphamate -   5=5.7-dihydroxy flavone -   6=5-hydroxy-flavone-7-sulphamate -   7=5.7-dihydroxy-4′-hydroxy-flavone -   8=5.7-dihydroxy flavanone-4′-flavanone sulphamate -   9=5,7-dihydroxy-4′-methoxy-isoflavone -   10=5-hydroxy-4′-methoxy-isoflavone-isoflavone-7-sulphamate

The formulae are presented in FIGS. 16 a, 16 b, 16 c, 17-22.

Synthesis

The sulphamate derivatives were prepared essentially as described previously (J. Med. Chem. 37: 219-21). In this regard, a solution of the appropriate flavone, isoflavone or flavanone in anhydrous DMF was treated with sodium hydride (60% dispersion; 1 equiv for 2 and 4; 2 equiv for 6, 8 and 10) at 0° C. under an atmosphere of N₂. After evolution of hydrogen had ceased, sulfamoyl chloride (2 equiv except for 8, 5 equiv) was added and the reaction mixture was poured into brine after warming to room temperature overnight and diluting with ethyl acetate. The organic fraction was washed exhaustively with brine, dried (MgSO₄), filtered and evaporated. The crude product obtained was purified by flash chromatography and recrystallisation to give the corresponding sulfamate.

Flavone 6-O-sulphamare (2)

6-Hydroxyflavone (1.0 g. 4.113 mmol) gave crude product (1.21 g) which was fractionated on silica (200 g) with ethyl acetate. Upon evaporation, the first fraction gave a creamy residue (760 mg. 58.2%) which was recrystallised in warm acetone/hexane (3:2) to give 2 as creamy rod-shaped crystals (557 mg). m.p. 190-191° C.; R_(f)s=0.71 (ethyl acetate). 0.51 (ethyl acette/hexane, 2:1). νmax (KBr) 3260, 3040, 1620, 1600, 1580, 1370, 1180 cm⁻¹; δ_(H) (acetone-d₆)6.917 (1H, s, C-3-H), 7.355 (2H, br s, exchanged with D₂O, —OSO₂NH ₂), 7.64 (3H, m, C-3′-H, C-4′-H and C-5′-H). 7.75 (1H, dd, J_(C-8-H,C-7-H)=9 Hz and J_(C-5-H,C-7-H)=3 Hz, C-7-H), 7.87 (1H, d, J_(C-7-H,C-8-H)=9 Hz, C-8H), 8.02 (1H, d, J_(C-7-H, C-5-H)=3 Hz, C-5-H) and 8.13 (2H, m, C-2′-H and C-6′-H). MS: m/z (E.I., rel. intensity) 317.0(11), 304.2(6), 238.0(96), 210.0(16), 187.1(14), 152.0(8), 136.0(100). Acc. MS (E.I.): m/z 317.0296, C₁₅H₁₁NO₅S requires 317.0358. Found C, 56.7; H, 3.44; N, 4.31. C₁₅H₁₁NO₅S requires C, 56.78; H, 3.49; N. 4.41%.

Flavone 7-O-Sulphamate (4)

7-Hydroxyflavone (700 mg, 2.938 mmol) gave crude product (770 mg) which was fractionated on silica (200 g) with ethyl acetate. Upon evaporation, the first fraction gave a light brown residue (132 mg) which was rectystallised in hot isopropyl alcohol to give 4 as white needle-shaped crystals (60 mg). m.p. 172-174° C. (dec.); R_(f)s=0.78 (ethyl acetate), 0.56 (ethyl acetate/hexane, 4.1); νmax (KBr) 3260, 3100, 1630, 1600, 1400, 1580, 1200, 1150 cm⁻¹; δ_(H) (DMSO-d₆/CDCl₃, ca. 1:20) 6.824 (1H, s, C-3-H), 7.396 (1H, dd, J_(C-5-H,C-6-H)=8.8 Hz and J_(C-8-H,C-6-H)=2.2 Hz, C-6-H), 7.47 (2H, br S, exchanged with D₂O, —OSO₂NH ₃), 7.55 (3H, m, C-3′-H, C-4′-H and C-5′-H), 7.639 (1H, d, J_(C-6-H,C-8-H)=2.2 Hz, C-8-H), 7.92 (2H, m, C-2′-H and C-6′-H) and 8.220 (1H, d, J_(C-6-H,C-5-H)=8.8 Hz, C-5-H). Found: C, 56.5; H, 3.36: N, 4.19. C₁₅H₁₁NO₅S requires C, 56.78; H. 3.49; N, 4.41%.

5-Hydroxyflavone 7-O-Sulphamate (6)

5,7-Dihydroxyflavone (1.0 g. 3.933 mmol) gave crude product (1.13 g) which was fractionated on silica (200 g) with chloroform/acetone (8:1). Upon evaporation, the second fraction gave a yellow residue (324 mg. 24.7%) which was recrystallised in ethyl acetate/hexane (1:1) to give 6 as yellow crystals (213 mg). m.p. 195-200° C. (dec.); R_(f)s=0.21. 0.25 and 0.44 for chloroform/acetone 12:1, 8:1 and 4:1 respectively: νmax (KBr) 3360, 3250, 2925-2850, 1650, 1610, 1380 cm⁻¹, δ_(H) (acetone-d₆) 6.75, 6.98, 7.17 (3H, three s, C-3-H, C-6-H, C-8-H), 7.63 (2H, br s, exchanged with D₂O, —OSO₂NH ₃), 7.65 (3H, m, C-3H, C-4′-H and C-5′-H), 8.15 (2H, d, J=7.7 Hz. C-2′-H and C-6′-H) and 13.0 (1H, br s, exchanged with D₂O, C-5-O-H). MS: m/z (+ve ion FAB in m-NBA, rel. intensity) 440.1(10), 389.3(10), 334.1[100, (M+H)⁺], 288.1(17), 255.0[25, (M+H-79)⁺]169.1(30). MS: m/z (−ve ion FAB in m-NBA. rel. intensity) 499.0(30), 484.1[14, (M-2H+153)⁻], 475.1(20), 443.1(24), 332.1[100, (M−H)⁻], 308.1(28), 274.1(20). 253.1[50, (M−H-79)⁻], 195.1(24). Acc. MS (+ve ion FAB in m-NBA): m/z 334.0392. C₁₅H₁₂NO₆S requires 334.0385, Found: C, 54.0; H, 3.39; N, 4.21. C₁₅H₁₁NO₆S requires C, 54.03; H, 3.33; N, 4.20%.

5,7-Dihydroxyflavanone 4′-O-Sulphamate (8)

4′,5,7-Trihydroxyflavanone (1.0 g. 3.675 mmol) gave crude product (965 mg) which was fractionated on silica (200 g) with ethyl acetatelhexane (4:1) to give a mixture of the starting flavanone and product. This mixture was further fractionated on silica (200 g) with chloroformn/acetone (4:1) and upon evaporation. the second fraction gave a pale yellow oil (345 mg, 34%) which solidified on standing. Subsequent recrystallisation of this solid in ethyl acetate/hexane (1:1) gave 8 as white crystals (259 m/g), m.p. 211-213° C.; R_(f)=0.21 (chloroformlacetone, 4:1); νmax (KBr) 3420, 3340, 3260, 3140, 1640, 1510, 1380, 1160 cm⁻¹; δ_(H) (acetone-d₆) 2.84 (1H, dd, J_(AB)=17.4 Hz and J_(2Z,eq)=3.1 Hz, C-3-H ₈), 3.19 (1H, dd, J_(8A)=16.9 Hz and J_(2B,2A)=12.8 Hz, C-3-H _(A)), 5.62 (1H, dd, J_(2A,eq)=3.1 Hz and J_(2A,2X)=12.8 Hz, C-2-H), 5.98 (1H, d, J=2.0 Hz, C-6-H or C-8-H), 6.01 (1H, d, J=2.0 Hz, C-6-H or C-8-H), 7.20 (2H, br s, exchanged with D₂O, —OSO₂NH ₂), 7.40 (2H, d, J=8.7 Hz, C-2′-H and C-6′-H), 7.66 (2H, d, J=8.7 Hz, C-3′-H and C-5′-H), 9.65 (1H, br s, C-7-OH) and 12.15 (1H, s, C-5-OH), MS: m/z (+ve ion FAB in m-NBA, rel. intensity) 352.0[100, (M+H)⁺], 288.1(10),272.1[14, (M-79)⁻], 255.2(9). 169.0(13). MS: m/z (−ve ion FAB in m-NBA, rel. intensity) 701.2(12), 606.2(10), 517.1(42), 504.1[20, (M+153)⁻], 473.2(10), 350.1[100, (M−H)⁻], 271.1[45. (M−H-79)⁻], 182.0(8). Acc

MS (+ve ion FAB in m-NBA): m/z 352.0496, C₁₅H₁₄NO₇S requires 352.0491. Found: C. 51.1; H, 3.68; N, 3.98. C₁₅H₁₂NO₇S requires C, 51.28: H, 3.73; N, 3.99%.

5-Hydroxy-4′-methoxyisoflavone 7′-O-sulphamate (10)

5,7-Dihydroxy-4′-methoxyisoflavone (800 mg, 2.817 mmol) gave crude product (650 mg) which was fractionated on silica (200 g) with chloroform/acetone (8:1). Upon evaporation, the second fraction gave a yellow residue (266 mg, 26%) which was recrystallised in ethyl acetate/hexane (1:1) to give 10 as yellow crystals (211 mg), m.p. 184-188° C.; R_(f)s=0.22 and 0.59 for chloroform/acetone 8:1 and 4:1 respectively; νmax (KBr) 3300-3020, 1660, 1610, 1400 cm⁻; δ_(H) (acetone-d₆) 3.86 (3H, s, —OCH ₃), 6.75 (1H, d, J=2.2 Hz, C-6-H or C-D8-H), 7.04 (3H, m, C-6-H or C-8-H and C-3′-H and C-5′-H), 7.49 (2H, br s, exchanged with D₂O, —OSO₂NH ₂), 7.58 (2H, d, J=7 Hz, C-2′-H and C-6′-H), 8.41 (1H, s, C-2-H), 13.04 (1H, br s, exchanged with D₂O, C-5-OH), MS: m/z (+ve ion FAB in m-NBA, rel. intensity) 393.3(12), 364.0[100. (M+H)⁺], 284.1[12, (M-79)⁺], 169.1(24), 134.0(22). MS: m/z (−ve ion FAB in m-NBA, rel. intensity) 529.1(25), 515.1[12, (M−H+153)⁻], 442.1(20), 362.1[100, (M−H)⁻], 308.1(34), 283.1[70, (M−H-79)⁻], 170.1(26). Acc.

MS (+ve ion FAB in m-NBA): m/z 364.0494, C₁₆H₁₄NO₇S requires 364.0491.

Found: C, 52.8; H, 3.65; N, 3.81. C₁₆H₁₃NO₇S requires C, 52.89; H, 3.61; N, 3.85%.

5-Hydroxy Isoflavone4′,7-O,O-Disulphamate (11) and 5,7-Dihydroxy Isoflavone-4′-O-Sulphamate (12)

4′,5,7-Trihydroxy isoflavone (0.5 g, 1.85 mmol) upon sulphamoylation gave a crude product (0.65 g) which was fractionated on silica (200 g) with chloroform/acetone (4:1), and upon evaporation the third fraction gave a light yellow residue (0.329 g, 51%) which was recrystallized in ethylacetate/hexane (1:2) to give compound (11) as beige crystals (0.197 g); m.p=>198° C. (dec); R_(f)s=0.14 and 0.24 for chloroform/acetone 4:1 and 2:1 respectively; ν^(max) (KBr) 3460 (—NH₂), 1650 (C═O), 1400 (—SO₂N—) cm⁻¹; δ_(H) (acetone-d₆) 6.78 (1H, d, J=2.2 Hz, C-6-H or C-8-H, 7.03 (1H, d, J=2.2 Hz, C-8-H or C-6-H), 7.4 (4H, br s, exchanged with D₂O, C4′-OSO₂NH, and C-7-OSO₂NH ₂), 7.43 (2H, d, J=8.4 Hz, C-3′H and C-6′-H or C-2′-H and C-6′-H and C-6′-H), 7.72 (2H, d, J=8.4 Hz, C-2′-H and C-6′-H or C-3′-H and C-5′-H), 8.51 (1H, s, C-2-H) and 12.93 (1H, s, C-5-OH). MS: m/z (+ve ion FAB in m-NBA, rel. intensity) 428.9 [100, (M+H)⁺], 350.0 [20, (M+H—SO₂NH₂)⁺], 272.1 [130. (M−H—SO₂NH₂)⁺]. MS: m/z (−ve ion FAB in m-NBA, rel. intensity) 426.9 [100, (M−H)⁻], 347.9 [95, (M−H—SO₂NH₂)⁻], 269.0 [30, (M−H—SO₂NH₂)⁻]. Acc. MS: m/z (FAB)⁺429.0083 C₁₅H₁₃N₂O₉S₂ requires 429.0063. Found C. 42.0; H, 2.91; N, 6.45; C₁₅H₁₂N₂O₉S₂ requires C, 42.06; H, 2.82; N, 6.54%.

The second fraction was collected and upon evaporation gave light yellow residue (0.112 g, 17%) which was recrystallized in ethylacetate/hexane (1:3) to give compound (12) as pale white crystals (0.068 g); m.p.=189-192° C. R_(f)s=0.23 and 0.33 for chloroform/acetone 4:1 and 2:1 respectively; ν^(max) (KBr) 3500-3300 (—NH₂), 3200 (H-bonded-OH), 1680 (C═O), 1610, 1400 (—SO₂N—)cm⁻¹; δ_(H) (acetone-d₆) 6.32 (1H, d, J=2.2 Hz, C-6-H or C-8-H), 6.46 (1H, d, J=2.2 Hz, C-8-H or C-6-H), 7.32 (2H, br s, exchanged with D₂O, —SO₂NH ₂), 7.42 (2H, t, J=8.4 Hz, C-3′-H and C-5′-H or C-2′-H and C-6′-H, 7.69 (2H, d, J=8.4 Hz, C-2′-H and C-6′-H or C-3′-H and C-5′-H), 8.31 (1H, s, C-2-H), 9.53 (1H, s, C-7-OH) and 12.9 (1H, s, C-5-OH), MS: m/z (+ve ion FAB in m-NBA, rel. intensity) 350.0 [100, (M+H)⁺], 271.1 [15, (M+H—SO₂NH₂)⁺]. MS: m/z (−ve ion FAB in m-NBA, rel. intensity) 347.9 [100, (M−H)⁻], 269.0 [20, (M−H—SO₂NH₂)⁻]. Acc. MS: m/z (FAB)⁺350.0347 C₁₅H₁₂NO₇S requires 350.0335. Found C, 51.0; H. 3.16: N. 3.90: C₁₅H₁₁NO₇S requires C, 51.58; H, 3.17; N, 4.01%.

Isoflavone4′,7-O,O-Disulphamate (13)

4′,7-Dihydroxy isoflavone (0.45 g, 1.77 mmol) upon sulphamoylation gave a crude product (0.769 g) which was fractionated on silica (200 g) with chloroformlacetone (4:1), and upon evaporation the second fraction gave a pale white residue (0.553 g. 72%) which was recrystallized in acetone/hexane (1:2) to give the compound (13) as white crystals (0.327 g); m.p.>195° C. (dec.); R_(f)s=0.21 and 0.40 for chloroform/acetone 4:1 and 2:1 respectively; ν^(max) (KBr) 3400 (—NH₂), 1640 (C═O), 1360 (—SO₂N—) cm⁻¹, δ_(H) (DMSO-d₆), 7.37 (2H, d, J=8.8 Hz. C-3′-H and C-5′-H or C-2′-H and C-6′-H, 7.42 (1H, dd, J_(C-6-H,C-8-H)=2.2 Hz, J_(C-6-H,C-5-H)=8.8 Hz, C-6-H), 7.7 (2H, d, J=8.8 Hz, C-2′-H and C-6′-H or C-3′-H and C-5′-H), 8.09 (2H, br s, exchanged with D₂O, —OSO₂NH ₂), 8.24 (1H, d, J=8.8 Hz, C-5-H, 8.36 (2H, br s, exchanged with D₂O, —OSO₂NH ₂), 8.63 (1H, s, C-2-H). MS: m/z (+ve ion FAB in m-NBA, rel. intensity) 412.9 [100, (M+H)⁺], 334.0 [25, (M+H—SO₂NH₂)⁺], 255.1 [20, (M+H—SO₂NH₂)⁺]. MS: m/z (−ve ion FAB in m-NBA, rel. intensity) 410.9 [100, (M−H)⁻, 332.0 (70, (M−H—SO₂NH₂)⁻], 253.0 [30, (M−H—SO₂NH₂)⁻]. Acc. MS: m/z (FAB)⁺413.0119 C₁₅H₁₃N₂O₈S₂ requires 413.0113.

Found C, 44.0; H, 2.94; N. 6.62; C₁₅H₁₂N₂O₈S₂ requires C, 43.69; H, 2.93; N, 6.79%.

Assay of Inhibition of Sulphatase and Aromatase Activities

Sulphatase inhibition was assessed using placental microsome (100,000 g) preparations or intact MCF-7 breast cancer cells as described previously. Placental microsomes were incubated with ³H E1S, adjusted to 20 μM with unlabelled substrate, in the absence or presence of inhibitor. (J Med Chem 37:219 21; Biochemistry 34:11508-14.)

Placental microsomes were also used to assess the aromatase inhibitory properties of the flavanoid sulphamates using a tritiated water release assay (J Steroid Biochem 24:1033-39). Further placental microsomes (200 μl) were incubated with [1β-³H] androstenedione. 60 nM and 1 mM NADPH in the absence or presence of inhibitor.

Inhibition of Sulphatase and Aromatase Activities

Inhibition of oestrone sulphatase and aromatase activities in placental microsomes by the flavanoid sulphamate derivatives is shown in the Table below.

% % CONCENTRATION INHIBITION INHIBITION COMPOUND μM Sulphatase Aromatase Flavone-6- 1 26.8 1 sulphamate 10 89.5 6.5 Flavone-7- 1 — 55 sulphamate 10 — 86 50 56.3 100 75.3 5-hydroxy 1 8 5 flavone-7- 10 21 76 sulphamate 5,7-dihydroxy 0.1 30.4 Not tested flavanone 4′- 1 79.1 Not tested sulphamate 10 98.1 Not tested 5-hydroxy-4′- 1 1 2 methoxy- 10 50.6 5 isoflavone-7- sulphamate

From the results, it can be seen that potent inhibition of sulphatase and aromatase activities was detected. For sulphatase inhibition this ranged from 21% at 10 μM by 5-hydroxy flavone-7-sulphamate, to 98% by 5,7-dihydroxy flavanone4′-sulphamate at 10 μM. Potent aromatase inhibition was also achieved ranging from 6.5% by flavone-6-sulphamate at 10 μM to 86% by flavone-7-sulphamate at 10 μM.

Further in Vitro Testing

The following Table presents in vitro data for three isoflavones that were tested.

IN VITRO ACTIVITY % Inhibition Concentration MCF-7 Placental Compound (μM) Cells Microsomes Isoflavone-5-hydroxy- 0.1 28 nd 4′,7-bissulphamate 1.0 90 nd 10.0 99 93 Isoflavone 5,7-dihydroxy- 0.1 23 nd 4′-sulphamate 1.0 83 nd 10.0 99 75 Isoflavone-4′,7- 0.1 89 nd bissulphamate 1.0 99 nd 10.0 99 99 nd = not done

In Vivo Testing

FIG. 24 presents in vivo inhibition of oestrone sulphatase activity in rat liver for two isoflavones according to the present invention. In this regard. BH22F1=5-hydroxy isoflavone4′,7-bissulphamate; BH22BF1=5,7-dihydroxy isoflavone-4′-sulphamate. Compounds were administered as a single 10 mg/Kg dose. Oestrone sulphatase activity was assayed in tissue samples obtained 24 h after drug administation.

Other modifications of the present invention will be apparent to those skilled in the art.

EXAMPLE 15

Preparative Methods

The preparation of various compounds in accordance with the present invention is illustrated in FIGS. 35 to 38. In these Figures, the curved lines attached to the phenyl rings represent the remainder of the ringed structure.

In Vitro Inhibition

The ability of compounds to inhibit oestrone sulphatase activity was assessed using either intact MCF-7 breast cancer cells or placental microsomes as previously described (Int. J. Cancer 1995, 62, 106-11.)

In this regard, the teachings of that earlier reference are as follows:

Inhibition of Steroid Sulphatase Activity in MCF-7 Cells by Oestrone-3-sulphamate

Steroid sulphatase is defined as: Steryl Sulphatase EC 3.1.6.2.

Steroid sulphatase activity was measured in vitro using intact MCF-7 human breast cancer cells. This hormone dependent cell line is widely used to study the control of human breast cancer cell growth. It possesses significant steroid sulphatase activity (MacIndoe et al. Endocrinology, 123, 1281-1287 (1988); Purohit & Reed, Int. J. Cancer, 50, 901-905 (1992)) and is available in the U.S.A. from the American Type Culture Collection (ATCC) and in the U.K. (e.g. from The Imperial Cancer Research Fund). Cells were maintained in Minial Essential Medium (MEM) (Flow Laboratories, Irvine, Scotland) containing 20 mM HEPES, 5% foetal bovine serum, 2 mM glutamine, non-essential amino acids and 0.075% sodium bicarbonate. Up to 30 replicate 25 cm² tissue culture flasks were seeded with approximately 1×10⁵ cells/flask using the above medium. Cells were grown to 80% confluency and medium was changed every third day.

Intact monolayers of MCF-7 cells in triplicate 25 cm² tissue culture flasks were washed with Earle's Balanced Salt Solution (EBSS from ICN Flow, High Wycombe, U.K.) and incubated for 34 hours at 37° C. with 5 pmol (7×10⁵ dpm) [6,7-³H]oestrone-3-sulphate (specific activity 60 Ci/mmol from New England Nuclear, Boston, Mass., U.S.A.) in serum-free MEM (2.5 ml) together with oestrone-3-sulphamate (11 concentrations: 0; 1 fM; 0.01 pM; 0.1 pM; 1 pM; 0.01 nM; 0.1 nM; 1 nM; 0.01 mM; 0.1 mM; 1 mM). After incubation each flask was cooled and the medium (1 ml) was pipetted into separate tubes containing [¹⁴C]oestrone (7×10³ dpm) (specific activity 97 Ci/mmol from Amersham International Radiochemnical Centre, Amersham, U.K.). The mixture was shaken thoroughly for 30 seconds with toluene (5 ml). Experiments showed that >90% [¹⁴C]oestrone and <0.1% [³H]oestrone-3-sulphate was removed from the aqueous phase by this treatment. A portion (2 ml) of the organic phase was removed, evaporated and the ³H and ¹⁴C content of the residue determined by scintillation spectrometry. The mass of oestrone-3-sulphate hydrolysed was calculated from the ³H counts obtained (corrected for the volumes of the medium and organic phase used, and for recovery of [¹⁴C]oestrone added) and the specific activity of the substrate. Each batch of experiments included incubations of microsomes prepared from a sulphatase-positive human placenta (positive control) and flasks without cells (to assess apparent non-enzmatic hydrolysis of the substrate). The number of cell nuclei per flask was determined using a Coulter Counter after treating the cell monolayers with Zaponin. One flask in each batch was used to assess cell membrane status and viability using the Trypan Blue exclusion method (Phllips, H. J. (1973) In: Tissue culture and applications, [eds: Kruse, D. F. & Patterson, M. K.]; pp. 406-408; Academic Press, New York).

Results for steroid sulphatase activity are expressed as the mean ±1 S.D. of the total product (oestrone+oestradiol) formed during the incubation period (20 hours) calculated for 10⁶ cells and, for values showing statistical significance, as a percentage reduction (inhlbition) over incubations containing no oestrone-3-sulphamate. Unpaired Student's t-test was used to test the statistical significance of results.

Inhibition of Steroid Sulphatase Activity in Placental Microsomes by Oestrone-3-sulphatase

Sulphatase-positive human placenta from normal term pregnancies (Obstetric Ward, St. Mary's Hospital, London) were thoroughly minced with scissors and washed once with cold phosphate buffer (pH 7.4, 50 mM) then re-suspended in cold phosphate buffer (5 ml/g tissue). Homogenisation was accomplished with an Ultra-Turrax homogeniser, using three 10 second bursts separated by 2 minute cooling periods in ice. Nuclei and cell debris were removed by centrifuging (4° C.) at 2000 g for 30 minutes and portions (2 ml) of the supernatant were stored at −20° C. The protein concentration of the supernatants was determined by the method of Bradford (Anal. Biochem., 72, 248-254 (1976)).

Incubations (1 ml) were carried out using a protein concentration of 100 mg/ml, substrate concentration of 20 mM [6,7-³H]oestrone-3-sulphate (specific activity 60 Ci/mmol from New England Nuclear, Boston, Mass., U.S.A.) and an incubation time of 20 minutes at 37° C. If necessary eight concentrations of compounds are employed: 0 (i.e. control); 0.05 mM; 0.1 mM; 0.2 mM; 0.4 mM; 0.6 mM; 0.8 mM; 1.0 mM. After incubation each sample was cooled and the medium (1 ml) was pipetted into separate tubes containing [¹⁴]oestrone (7×10³ dpm) (specific activity 97 Ci/mmol from Amersham International Radiochemical Centre, Amersham, U.K.). The mixture was shaken thoroughly for 30 seconds with toluene (5 ml). Experiments showed that >90% [¹⁴C]oestrone and <0.1% [3H]oestrone-3-sulphate was removed from the aqueous phase by this treatment. A portion (2 ml) of the organic phase was removed, evaporated and the ³H and ¹⁴C content of the residue determined by scintillation spectrometry. The mass of oestrone-3-sulphate hydrolysed was calculated from the ³H counts obtained (corrected for the volumes of the medium and organic phase used, and for recovery of [¹⁴C]oestrone added) and the specific activity of the substrate.

For the present invention, the percentage inhibition for the series of EMATE analogues tested in either MCF-7 cells or placental microsomes is shown in Table 1, below.

In Vivo Studies

Using 17-deoxy oestrone-3-O-sulphamate (NOMATE, FIG. 28, Formula IV where X═—OSO₂NH₂, Y═—CH₂— and R₁ and R₂═H, and FIG. 36) as a representative example, the ability of this compound to inhibit oestrone sulphatase activity in vivo was examined in rats. The oestrogenicity of this compound was examined in ovariectomised rats. In this model compounds which are oestrogenic stimulate uterine growth.

(i) Inhibition of Oestrone Sulphatase Activity in Vivo

NOMATE (0.1 mg/Kg/day for five days) was administered orally to rats with another group of animals receiving vehicle only (propylene glycol). At the end of the study samples of liver tissue were obtained and oestrone sulphatase activity assayed using ³H oestrone sulphate as the substrate as previously described (Int. J. Cancer, 1995, 62, 106-11).

As shown in FIG. 39, administration of this dose of NOMATE effectively inhibited oestrone sulphatase activity by 98% compared with untreated controls.

(ii) Lack of in Vivo Oestrogenicity

NOMATE (0.1 mg/Kg/day for five days) was administered orally to rats with another group of animals receiving vehicle only (propylene glycol). At the end of the study uteri were obtained and weighed with the results being expressed as uterine weight/whole body weight×100.

As shown in FIG. 40, administration of NOMATE at the dose tested, but had no significant effect on uterine growth, showing that at his dose the compound is not oestrogenic.

TABLE 1 Inhibition of Oestrone Sulphatase Activity in MCF-7 Cells or Placental Microsomes by EMATE Analogues % Inhibition (Mean) Concentration MCF-7 Placental Inhibitor Tested (mM) Cells Microsomes 2-n-propyl EMATE 0.1 41.1 — 1 83.1 21.9 10 92.2 43.2 25 — 47.5 50 — 61.1 100 — 69.2 4-n-propyl EMATE 1 — 13.7 10 — 10.2 25 — 15.7 50 — 16.3 100 — 23.7 2,4-n-dipropyl EMATE 0.1  6.6 — 1 10.6 — 2-allyl EMATE 0.01 23.2 — 0.1 76.1 — 1 94.2 45.6 10 93.7 65.4 25 — 75.3 50 — 86.6 100 — 89.6 4-allyl EMATE 1 — 29.1 (approx 75%) 10 — 54.2 25 — 59.0 50 — 65.1 100 — 71.9 2,4-di-allyl EMATE — — — 2-methoxy EMATE 0.1 96.0 — 1 93.6 — 10 96.2 99.0 50 — 99.7 100 — 99.7 2-nitro EMATE 0.05 — 44.5 0.5 — 93.9 5 — 99.0 50 — 99.4 4-nitro EMATE 20 — 99.0 NOMATE 0.1 96.4 97.2 (17-deoxy EMATE) 1 99.1 99.5 10 99.7 99.5 25 99.7 99.7 — = not tested Irreversible time- and concentration-dependent inhibition is assumed for these compounds in keeping with established precedent (Biochemistry, 1995, 34, 11508-11).

Other modifications of the present invention will be apparent to those skilled in the art. 

1. A pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and a pharmaceutically effective amount of a compound of the formula (II)

wherein R₁ and R₂ are independently H or C₁-C₅ alkyl, and at least one of R₁ and R₂ is H; and the ring system ABCD represents a steroid nucleus, selected from the group consisting of dehydroepiandrosterone, oestrone, 2-OH-oestrone, 7α-OH-oestrone, 2-methoxy-oestrone, 16α-OH-oestrone, 4-OH-oestrone, 16β-OH-oestrone, 6α-OH-oestrone, 2-OH-17β-oestradiol, 6α-OH-17β-oestradiol, 16β-OH-7α-oestradiol, 17β-oestradiol, 2-methoxy-17β-oestradiol, 7α-OH-17β-oestradiol, 16α-OH-17α-oestradiol, 17α-ethinyl-17β-oestradiol, 4-OH-17β-oestradiol, 16α-OH-17α-oestradiol, 17α-oestradiol, oestradiol, 4-OH-oestradiol, 2-OH-oestradiol, 6α-OH-oestradiol, 2-methoxy-oestradiol, 7α-OH-oestradiol, 6α-OH-dehydroepiandrosterone, 16α-OH-dehydroepiandrosterone, 7α-OH-dehydroepiandrosterone, and 16β-OH-dehydroepiandrosterone, wherein said compound is an inhibitor of an enzyme having steroid sulphatase activity (EC 3.1.6.2); and wherein when the sulphamic acid ester group of said compound is replaced with a sulphate group to form a sulphate compound and incubated with a steroid sulphatase enzyme (EC 3.1.6.2) at a pH 7.4 and 37° C. it provides a K_(m) value of less than 50 μM, or a pharmaceutically acceptable salt thereof.
 2. The pharmaceutical composition of claim 1 wherein the steroid nucleus has the ring system ABCD of oestrone.
 3. The pharmaceutical composition of claim 1 wherein the steroid nucleus has the ring system ABCD of 17β-oestradiol.
 4. The pharmaceutical composition of claim 1 wherein the steroid nucleus has the ring system ABCD of 17α-ethinyl-17β-oestradiol.
 5. The pharmaceutical composition of claim 1 wherein the steroid nucleus has the ring system ABCD of 17α-oestradiol.
 6. The pharmaceutical composition of claim 1 wherein the steroid nucleus has the ring system ABCD of oestradiol.
 7. The pharmaceutical composition of claim 1 wherein R₁ and R₂ are H.
 8. The pharmaceutical composition of claim 2 wherein R₁ and R₂ are H.
 9. The pharmaceutical composition of claim 3 wherein R₁ and R₂ are H.
 10. The pharmaceutical composition of claim 4 wherein R₁ and R₂ are H.
 11. The pharmaceutical composition of claim 5 wherein R₁ and R₂ are H.
 12. The pharmaceutical composition of claim 6 wherein R₁ and R₂ are H.
 13. A purified compound of the formula (II)

wherein R₁ and R₂ are independently H or C₁-C₅ alkyl, and at least one of R₁ and R₂ is H; and the ring system ABCD represents a steroid nucleus, selected from the group consisting of dehydroepiandrosterone, oestrone, 2-OH-oestrone, 7α-OH-oestrone, 2-methoxy-oestrone, 16α-OH-oestrone, 4-OH-oestrone, 16β-OH-oestrone, 6α-OH-oestrone, 2-OH-17β-oestradiol, 6α-OH-17β-oestradiol, 16β-OH-7α-oestradiol, 17β-oestradiol, 2-methoxy-17β-oestradiol, 7α-OH-17β-oestradiol, 16α-OH-17β-oestradiol, 17α-ethinyl-17β-oestradiol, 4-OH-17β-oestradiol, 16α-OH-17α-oestradiol, 17α-oestradiol, oestradiol, 4-OH-oestradiol, 2-OH-oestradiol, 6α-OH-oestradiol, 2-methoxy-oestradiol, 7α-OH-oestradiol, 6α-OH-dehydroepiandrosterone, 16α-OH-dehydroepiandrosterone, 7α-OH-dehydroepiandrosterone, and 16β-OH-dehydroepiandrosterone, wherein said compound is an inhibitor of an enzyme having steroid sulphatase activity (EC 3.1.6.2); and wherein when the sulphamic acid ester group of said compound is replaced with a sulphate group to form a sulphate compound and incubated with a steroid sulphatase enzyme (EC 3.1.6.2) at a pH 7.4 and 37° C. it provides a K_(m) value of less than 50 μM, or a pharmaceutically acceptable salt thereof.
 14. The purified compound of claim 13 wherein the steroid nucleus has the ring system ABCD of oestrone.
 15. The purified compound of claim 13 wherein the steroid nucleus has the ring system ABCD of 17β-oestradiol.
 16. The purified compound of claim 13 wherein the steroid nucleus has the ring system ABCD of 17α-ethinyl-17β-oestradiol.
 17. The purified compound of claim 13 wherein the steroid nucleus has the ring system ABCD of 17α-oestradiol.
 18. The purified compound of claim 13 wherein the steroid nucleus has the ring system ABCD of oestradiol.
 19. The purified compound of claim 13 wherein R₁ and R₂ are H.
 20. The purified compound of claim 14 wherein R₁ and R₂ are H.
 21. The purified compound of claim 15 wherein R₁ and R₂ are H.
 22. The purified compound of claim 16 wherein R₁ and R₂ are H.
 23. The purified compound of claim 17 wherein R₁ and R₂ are H.
 24. The purified compound of claim 18 wherein R₁ and R₂ are H.
 25. A pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and a pharmaceutically effective amount or a compound of the formula (II)

wherein R₁ and R₂ are independently H or C₁-C₅ alkyl; and the ring system ABCD represents a steroid nucleus, selected from the group consisting of dehydroepiandrosterone, 2-OH-oestrone, 7α-OH-oestrone, 2-methoxy-oestrone, 16α-OH-oestrone, 4-OH-oestrone, 16β-OH-oestrone, 6α-OH-oestrone, 2-OH-17β-oestradiol, 6α-OH-17β-oestradiol, 16β-OH-7α-oestradiol, 17β-oestradiol, 2-methoxy-17β-oestradiol, 7α-OH-17β-oestradiol, 16α-OH-17β-oestradiol, 4-OH-17β-oestradiol, 16α-OH-17α-oestradiol, 17α-oestradiol, oestradiol, 4-OH-oestradiol, 2-OH-oestradiol, 6α-OH-oestradiol, 2-methoxy-oestradiol, 7α-OH-oe 6α-OH-dehydroepiandrosterone, 16α-OH-dehydroepiandrosterone, 7α-OH-dehydroepiandrosterone, and 16β-dehydroepiandrosterone. wherein said compound is an inhibitor of an enzyme having steroid sulphatase activity (EC 3.1.6.2); and wherein when the sulphamic acid ester group of said compound is replaced with a sulphate group to form a sulphate compound and incubated with a steroid sulphatase enzyme (EC 3.1.6.2) at a pH 7.4 and 37° C. it provides a K_(m) value of less than 50 μM, or a pharmaceutically acceptable salt thereof.
 26. The pharmaceutical composition of claim 25 wherein the steroid nucleus has the ring ABCD of 17β-oestradiol.
 27. The pharmaceutical composition of claim 25 wherein the steroid nucleus has the ring ABCD of 17α-oestradiol.
 28. The pharmaceutical composition of claim 25 wherein the steroid nucleus has the ring system ABCD of oestradiol.
 29. The pharmaceutical composition of claim 25 wherein at least one of R₁ and R₂ is H.
 30. The pharmaceutical composition of claim 26 wherein at least one of R₁ and R₂ is H.
 31. The pharmaceutical composition of claim 24 wherein at least one of R₁ and R₂ is H.
 32. The pharmaceutical composition of claim 28 wherein at least one of R₁ and R₂ is H.
 33. The pharmaceutical composition of claim 25 wherein R₁ and R₂ are H.
 34. The pharmaceutical composition of claim 26 wherein R₁ and R₂ are H.
 35. The pharmaceutical composition of claim 27 wherein R₁ and R₂ are H.
 36. The pharmaceutical composition of claim 28 wherein R₁ and R₂ are H.
 37. A purified compound of the formula (II)

wherein R₁ and R₂ are independently H or C₁-C₅ alkyl; and the ring system ABCD represents a steroid nucleus, selected from the group consisting of dehydroepiandrosterone, 2-OH-oestrone, 7α-OH-oestrone, 2-methoxy-oestrone, 16α-OH-oestrone, 4-OH-oestrone, 16β-OH-oestrone, 6α-OH-oestrone, 2-OH-17β-oestradiol, 6α-OH-17β-oestradiol, 16β-OH-7α-oestradiol, 17β-oestradiol, 2-methoxy-17β-oestradiol, 7α-OH-17β-oestradiol, 16α-OH-17β-oestradiol, 4-OH-17β-oestradiol, 16α-OH-17α-oestradiol, 17α-oestradiol, oestradiol, 4-OH-oestradiol, 2-OH-oestradiol, 6α-OH-oestradiol, 2-methoxy-oestradiol, 17α-OH-o 6α-OH-dehydroepiandrosterone, 16α-OH-dehydroepiandrosterone, 7α-OH-dehydroepiandrosterone, and 16β-OH-dehydroepiandrosterone. wherein said compound is an inhibitor of an enzyme having steroid sulphatase activity (EC 3.1.6.2); and wherein when the sulphamic acid ester group of said compound is replaced with a sulphate group to form a sulphate compound and incubated with a steroid sulphatase enzyme (EC 3.1.6.2) at a pH 7.4 and 37° C. it provides a K_(m) value of less than 50 μM, or a pharmaceutically acceptable salt thereof.
 38. The purified compound or claim 37 wherein the steroid nucleus has the ring system ABCD of 17β-oestradiol.
 39. The purified compound of claim 37 wherein the steroid nucleus has the ring system ABCD of 17α-oestradiol.
 40. The purified compound of claim 37 wherein the steroid nucleus has the ring system ABCD of oestradiol.
 41. The purified compound of claim 37 wherein at least one of R₁ and R₂ is H.
 42. The purified compound of claim 38 wherein at least one of R₁ and R₂ is H.
 43. The purified compound of claim 39 wherein at least one of R₁ and R₂ is H.
 44. The purified compound of claim 40 wherein at least one of R₁ and R₂ is H.
 45. The purified compound of claim 37 wherein R₁ and R₂ are H.
 46. The purified compound of claim 38 wherein R₁ and R₂ are H.
 47. The purified compound of claim 39 wherein R₁ and R₂ are H.
 48. The purified compound of claim 40 wherein R₁ and R₂ are H. 